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Abortion In Costa Rica Wikipedia

Accordingly, almost all doctors will not carry out an abortion for any reason at all. [8] According to a survey made by the University of Costa Rica whilst most Costa Rican support therapeutic abortion (55%) very few support completely free abortion (only 11%). [9] [10] The poll showed that 55% support abortion to save the mother’s life, against 45% who oppose. 49% supports it in case of non-life threatening health problems against 39%, 43% in case the fetus has life-incompatible malformation versus 49% against, only 29% supports it in case of pregnancy of a child versus 57% against, only 28% in cases of rape against 61% opposing, and only 11% supports only on the woman’s request against 78% opposing it.
Neurotrophic Keratitis Wikipedia

Topical treatment with murine NGF showed to promote recovery of epithelial integrity and corneal sensitivity in NK patients. [28] Recently, a recombinant human nerve growth factor eye drop formulation has been developed for clinical use. [29] Cenegermin , a recombinant form of human NGF, has recently been approved in Europe in an eye drop formulation for neurotrophic keratitis. [30] Cenegermin as an eye drop formulation for treatment of NK is approved by FDA in August 2018 See also [ edit ] Keratitis Cornea Rare disease References [ edit ] ^ Bonini S, Rama P, Olzi D, Lambiase A, Neurotrophic keratitis.

NGF, TAC1, TMSB4X, TYRP1, NRP1, TBPL1, SEMA3C
- Neurotrophic Keratopathy Orphanet
  
  Neurotrophic keratopathy is a rare degenerative disease of the cornea characterized by reduction or loss of corneal sensitivity that can be asymptomatic or present with red-eye and, during the early stages of the disease, a minor decrease in visual acuity. It eventually leads to loss of vision. Epidemiology No epidemiological data are available. However, prevalence can be estimated at around 1/2,380 in Europe. Clinical description Neurotrophic keratopathy (NK) most commonly occurs in adults, and rarely presents in children. It is often asymptomatic, but early signs can include red-eye, blurred vision, and decreased visual acuity. As the disease progresses, epithelial defects and corneal ulcers may develop; corneal scarring and astigmatism can lead to further reduction of visual function.
Farmer's Lung Wikipedia

"Farmer's Lung Disease" . Canadian Family Physician . 28 : 1817–20. PMC 2306727 . PMID 21286564 . ^ a b Grant IW, Blyth W, Wardrop VE, Gordon RM, Pearson JC, Mair A (February 1972).

LTA, PSMB7, TNF, CPP
- Farmer's Lung Disease Orphanet
  
  Farmer's lung disease is the main form of occupational hypersensitivity pneumonitis (see this term), caused by chronic inhalation of microorganisms, often thermophilic actinomycetes and less commonly saccharopolyspora rectivirgula , living in mouldy hay, straw, or grain. It is characterized by variable degrees of dyspnea, cough, tiredness, headaches and occasional fever/night sweats, with acute, sub-acute or chronic clinical course
Bonnet–dechaume–blanc Syndrome Wikipedia

"Wyburn-Mason syndrome: an unusual presentation of bilateral orbital and unilateral brain arteriovenous malformations". Pediatric Radiology . 28 (3): 161. doi : 10.1007/s002470050319 .
- Wyburn-Mason Syndrome Orphanet
  
  Wyburn-Mason syndrome or Bonnet-Dechaume-Blanc syndrome is characterized by the association of arteriovenous malformations of the maxilla, retina, optic nerve, thalamus, hypothalamus and cerebral cortex. Epidemiology The prevalence is not known but it is very rare: fewer than 100 cases have been reported in the literature to date. The sex ratio is even. Clinical description Malformations appear successively, sometimes over several tens of years. Neurological clinical signs include: progressive neurological deficits depending on the location of the malformation, epilepsy or cephalalgia. These symptoms result in venous congestion and hemorrhage. Psychomotor delay in childhood is not common.
- Wyburn-Mason Syndrome Gard
  
  Wyburn Mason's syndrome is a condition in which blood vessels do not form correctly in both the retina of one eye and a part of the brain. These malformed blood vessels are called arteriovenous malformations (AVM). Wyburn Mason's syndrome is present from birth (congenital) and the cause is unknown. Individuals with this condition may have additional AVMs in other parts of the body, particularly the face. The symptoms of this condition are quite variable and depend on the size, location, and shape of the AVMs.
Dyssynergia Wikipedia

Archived from the original on 2011-08-28 . Retrieved 2011-05-12 . ^ "National Institute of Neurological Disorders and Stroke" .

CACNA2D2, CACNA1A, NPC1, SCN8A, ABCB7, SLC2A1, UROC1, GABRA1, HCN1, PIBF1, TUBB4A, CP, CACNB4, SOX2, PUM1, EGR3, ATP7A, ARCN1, ADPRS, GABRA4, YME1L1, PITRM1, RARS1, AP2M1, HK1, TWNK, SETX, POLG, ATXN3, ATM, PRNP, APTX, ITPR1, TTPA, TBP, ATP1A3, SPTBN2, ATP6, COQ8A, KCNA1, SIL1, PNKP, PNPLA6, SPG7, CA8, CSTB, COX8A, COX20, KCNA2, AARS2, GOSR2, PMM2, PEX10, SCN1A, DNAJC19, C9orf72, OPA1, MECP2, ATP2B3, PSEN1, TDP1, TTR, KCNJ10, SLC1A3, DLD, PLEKHG4, CNTNAP2, ATN1, SAMD9L, NKX2-1, EBF3, AIFM1, RUBCN, GALT, ITM2B, PRF1, ERCC4, GFAP, GJB1, GLB1, SLC52A2, DNM1L, SNX14, VPS13D, TSFM, PIK3CA, TRNE, TINF2, ND4, MVK, COX2, PIK3R5, ATP13A2, LMNB1, TDP2, ARSG, WWOX, ATP8A2, CHP1, APOB, ANK1, DARS2, SPG11, GSN, POLR3B, OPA3, AARS1, PLA2G6, STXBP1, UBE3A, TPP1, TRPC3, CLN5, PRRT2, DAB1, VAMP1, TRAK1, CEP164, SUCLG1, USH2A, DHX30, SLC6A19, RPIA, MAST1, UBAC2, FASTKD2, CNKSR2, CLRN1, KLLN, PET100, NEXMIF, TREX1, VHL, POLR3A, TUBB2B, SDCCAG8, NPC2, SLC35A1, NDUFS7, CIB2, SEC23B, VLDLR, ZNF423, MAPK8IP3, KIF1B, SPART, TCF20, TCN2, TERC, NSMF, NECAP1, PARS2, NDUFAF3, TERT, WHRN, TGFB1, COG4, FLRT3, TK2, SPIDR, ZFYVE26, ETHE1, ABCA5, TLR4, MED13L, SYNE1, SZT2, RPGRIP1L, IL12A-AS1, DMXL2, KIAA0556, VPS13A, MLC1, PMPCA, TOMM40, SLC30A9, WFS1, KIF7, BMP15, IQCB1, KLRC4, ZNF592, SDHAF1, POLR1C, MPDU1, PIGL, OFD1, PEX16, HS6ST1, CHCHD10, SNAP29, ALG11, PEX3, SLC6A5, NHLRC1, CTDP1, ELP1, NOL3, SGPL1, DCHS1, ST3GAL5, SYNJ1, SYNGAP1, CTSF, FGF17, HESX1, DPM1, CISD2, SUCLA2, FEZF1, AP3B2, PEX11B, ZNF142, SNORD118, NSD2, SEMA3A, MICU1, NELFA, ABCA7, GPHN, LRPPRC, RAD50, XPA, XPC, YWHAE, YWHAG, USH1C, SCO2, CEP104, AP5Z1, TUBA1A, TELO2, AGRN, KIAA0753, ALDH5A1, KIAA0586, FRMPD4, EPM2A, NUP214, PDHX, TCTN3, IFT140, AAAS, ABHD12, CEP120, TRAF3IP1, CEP290, TCTN2, UBA5, DHDDS, PDZD7, STN1, PANK2, CTC1, HYLS1, SRD5A3, ARMC9, NUBPL, DNAJC5, SLC19A3, COL18A1, SPRY4, C19orf12, CSPP1, ROGDI, CEP78, SLC13A3, SLC5A7, PROK2, RNASEH1, TRAPPC11, CDH23, HEPACAM, ARV1, ACD, FAT4, TMEM237, PCDH15, CPLANE1, NDUFAF5, CCDC28B, TMEM231, TCTN1, ADGRV1, TMEM107, PTPN22, MICOS13, SLC52A3, NUS1, ARL13B, RNF168, TRAPPC6B, USH1G, WDR81, NDUFA11, STX1B, SYT2, NAXE, PROKR2, TANGO2, NAGS, NDUFAF6, BEAN1, SLC46A1, TUBB, COA8, PIGY, COG8, NKX6-2, KISS1R, PIGO, ATAD1, WDR73, COX14, LYRM7, CEP41, TMEM67, C12orf65, ATPAF2, RFT1, NDUFAF2, PGAP3, PIGS, WDR19, CC2D2A, HACE1, TMEM216, TPRKB, SEPSECS, ABHD5, MECR, NDUFAF1, TACO1, GLRX5, TIMMDC1, ALG6, ACTL6B, TMEM138, PIGT, TBCE, CCDC141, OTUD6B, PTRH2, RRM2B, GMPPA, PCDH19, UQCRQ, SACS, SLC17A5, BSCL2, CYFIP2, TPK1, NPHP3, B9D1, INVS, GMPPB, COQ2, PGAP2, IL23R, FLVCR1, NDUFAF4, SUMF1, PSMC3IP, SUFU, RTEL1, ERAP1, TMEM126B, PIGV, PEX26, FRMD4A, WDR11, NAXD, MBD5, LMBRD1, INPP5E, INPP5K, NPHP4, MRPS22, PRDM8, MFSD8, NUP107, GJC2, MCOLN1, CHD7, SLC39A4, FOXRED1, ATAD3A, ADA2, RIPK4, NANS, TREM2, RNF216, NDUFB11, IL17RD, AHI1, SLC25A42, PIGG, MKS1, SLC13A5, TMEM70, CLN6, PIGW, FAM149B1, VRK1, TBCD, TRNK, COL13A1, MTTP, RNR1, TRNF, TRNH, TRNI, CCR1, ND6, TRNL1, TRNN, TRNP, TRNQ, TRNS1, TRNS2, COX6B1, ND5, KIT, ATP8, LETM1, TAT, LY6E, MEFV, COX15, MPV17, COX1, ND4L, COX3, CYTB, ND1, COX10, ND2, ND3, TRNW, MYD88, CLTC, NONO, NDUFS6, NDUFS8, ERCC3, NDUFV2, NEU1, NF2, PNP, ERCC8, NPHP1, NTRK2, OGDH, OTC, PAFAH1B1, PARN, NDUFS4, NDUFV1, NDUFS3, CHAT, NDUFS2, NDUFS1, NDUFB10, NDUFB9, NDUFB8, NDUFB3, NDUFA6, NDUFA1, CHD2, LYST, MYO9A, MYO7A, MYO5A, CPS1, KCNJ11, PCNA, GBA, GABRB3, EDNRB, GABRD, DYRK1A, GABRG2, GAMT, DUSP6, GABRB2, GBE1, GCK, GJA1, GCLC, DNMT1, GLRA1, EEF1A2, GABRB1, KCNB1, FOXI1, ERCC2, ERCC6, BPTF, FGF8, FGF12, FGFR1, EPRS1, EPB42, FMR1, FXN, CLN8, FSHR, FTL, NR5A1, GLRB, DNASE1L3, DNM1, CTSD, DCX, HMGCL, HNRNPH2, DCC, DBT, CYP27A1, CTNNA2, SARDH, IL10, IL12A, INS, PDX1, ANOS1, CSF1R, HLCS, HLA-DQB1, HLA-DQA1, HLA-B, HIC1, HEXB, DDB2, HARS1, GSS, DGUOK, DHFR, GRIN2D, GRIN2B, DKC1, GRN, DLAT, GPI, PAX6, CDC42, ERCC5, KIF1A, ARSA, RORA, ASL, ASS1, ATP1A2, SMPD1, PEX5, ATP6V1A, PEX2, PEX19, PTS, SNAI2, PTEN, AUH, PSEN2, APC, HTRA1, SNAP25, PRPS1, SORL1, BCKDHA, SOX10, SMARCB1, SARS1, PPT1, SCN3A, SDHD, SLC1A2, FAS, SLC4A1, SDHC, SDHB, SDHA, SCO1, SLC6A1, SCN9A, SCN2A, ARL3, SCN1B, ATXN8OS, SLC6A8, ATXN2, SLC12A3, SLC16A2, SLC18A3, SLC25A1, AKT1, ATXN1, SPAST, BBS1, PPP3CA, SLC26A4, C4A, PEX13, PEX12, PEX7, PEX6, PEX1, BCKDHB, ACAT1, ACADM, BTD, CACNA1B, PDGFB, SUOX, ABCC8, PDE6D, SURF1, SYT1, TACR3, PEX14, APP, PGM3, PLP1, BCS1L, SPR, STAT4, PGK1, STAT3, ACO2, SPTB, PHYH, SPTA1, ATXN7, AFP, ZFYVE9, SAR1A, AFG3L2, STUB1, TPO, GRM1, PDYN, CAPN1, PPP2R2B, CASP3, TGM6, EIF2B1, MRE11, FGF14, SLC9A6, CBLL2, PRND, HSD17B4, PRKCG, PRKN, MSTO1, MUL1, ATCAY, KCNC1, IREB2, GRID2, EIF2S2, EIF2B2, SLC9A1, EIF2B4, HTT, DOCK3, CERNA3, ACHE, GBA2, SOD1, ANO10, XRCC1, TP53, KCNC3, ATXN10, MAPK1, AR, PDHA1, RELN, SQSTM1, NUP93, CAMTA1, RFC1, PCYT1A, PRICKLE1, CTBP1, SAMD9, IGFALS, TSHZ1, USP14, C20orf181, BRCA1, ENO2, ACR, CDKN1A, CDC25C, BDNF, MINDY3, CDK1, MEF2B, CCND1, MIR3191, KRIT1, SCA37, CBLN1, CBLN4, HT, ERBB2, TTBK2, FMR1-IT1, CALM3, CALM2, BCL6, ALK, ATXN7L3B, CRK, ARSH, LMNB2, DAP, ABCD1, SLC25A46, TIMM8A, ALAS2, MAPK14, COA6, CRMP1, CHD6, CALM1, MARS2, ACTB, CRH, SCA18, ARMH1, SLC9C2, ADGRB3, NLRP3, SCA26, PARP1, FBXO32, XRCC6P5, CHRNA4, ZUP1, PRUNE2, LIG3, CAMKMT, PIK3CG, ARHGEF2, RNASE2, RFX3, PPT2, GRAP2, ATG5, PSMD7, KIF20B, RGS6, PKN1, MTSS1, POLD1, PLS3, PIK3CD, CILK1, PIK3CB, RABEPK, LANCL1, WARS2, NOP56, AHSA1, KHDRBS1, CPLX1, UTS2, EBNA1BP2, SLC7A9, CHEK2, PAH, RPS4X, S100B, TRPA1, HSPB3, SYP, TGM2, ELOVL4, TOP1, TOP2A, TPM3, TRH, TRIO, TRPC1, SPTBN1, TUBB2A, UCHL1, UCN, UTRN, ABCA2, SOX4, ZIC1, ZIC2, AIMP2, CCDC6, SLC6A3, CUL4B, SGCG, SEL1L, DENR, TP63, CACNA1G, MGLL, OPHN1, FGF9, GOLGA2, IFNG, HSPD1, HSPB2, HSPB1, HSPA4, HMBS, CWF19L1, UEVLD, CXCL2, GRM5, NLRP2, GRIN2A, GRB2, GNAL, OGG1, GLUD2, SLC12A9, GH1, TBC1D24, NUFIP2, KLHL1, TP53INP2, GAA, ANO3, FUS, PINK1, FRAXA, FOXO3, PANK1, IFRD1, MAP3K20, IL9, NTRK1, FAN1, NPY, NFASC, NCDN, MTCL1, BRD4, NBN, DAPK2, SUN2, GCA, MTO1, RNF19A, POLDIP2, FGF21, SEZ6L2, ANKRD1, MID1, SMAD2, RPSA, KIF5B, KCNN3, KCNMA1, KCNC2, RNF138, KCNA6, KCNA5, H3P28
- Ataxia Mayo_clinic
  
  Overview Ataxia describes poor muscle control that causes clumsy voluntary movements. It may cause difficulty with walking and balance, hand coordination, speech and swallowing, and eye movements. Ataxia usually results from damage to the part of the brain that controls muscle coordination (cerebellum) or its connections. Many conditions can cause ataxia, including alcohol misuse, stroke, tumor, brain degeneration, multiple sclerosis, certain medications and genetic disorders. Treatment for ataxia depends on the cause. Adaptive devices, such as walkers or canes, might help maintain independence.
Urogenital Fistula Wikipedia

The average age of a woman who develops a fistula due to prolonged labor is 28 years old. The average age of a woman who develops a fistula from other causes is 42 years old. [8] Women with a small pelvis are more likely to develop a fistula.

LFNG, OCRL, RET, ITGA8, RECQL4, DLL3, FGF20, GREB1L, HES7, RIPPLY2, MESP2
Fusarium Patch Wikipedia

Controlling Fusarium Patch Disease. GreenMaster 2nd ser. 28.April/May (1994): 16+. Turfgrass Information File.
Forced Abortion Wikipedia

"Chinese to Prosecute Peasant Who Resisted One-Child Policy" . The Washington Post . Retrieved 28 April 2010 . ^ Forced abortion sparks outrage, debate in China CNN , June 2012 ^ Jerry Dunleavy (July 09, 2020).
Stereotypy Wikipedia

Elephant deaths at zoos reignite animal debate . 2005-02-28 [Retrieved 2006-05-30]. Reuters. ^ Christie, Julie Christie (2008).

MEF2C, TRH, CRH, RERE, CHMP2B, POGZ, WASHC4, ADNP, AP4E1, TARDBP, FRRS1L, CIZ1, RTTN, CNTNAP2, TNIK, FOXP1, DCPS, SLC45A1, CRBN, RSRC1, FGFRL1, TREM2, NLGN3, IQSEC2, MAN1B1, CC2D1A, TUBB3, AIMP1, NRXN1, MED23, ATRX, HDAC4, HUWE1, CERT1, WARS2, SLC9A6, AP4S1, DEAF1, NPC2, TBR1, AP4B1, RAI1, KDM5B, CPLX1, KPTN, TMEM106B, NSUN2, AP4M1, SIK1, ALKBH8, PRRT2, NACC1, RAB39B, TRAPPC6B, METTL23, HGSNAT, B3GALNT2, NAGS, MED25, SPATA5, ARID2, FLCN, C9orf72, EBF3, CHAMP1, NAT8L, NEXMIF, TRAPPC9, LMAN2L, LINS1, PRDM16, ELP2, TBC1D23, MBD5, FMN2, C12orf4, THOC2, NLGN4X, BCORL1, IRF2BPL, TTI2, MBOAT7, RNASEH2B, FBXO31, EHMT1, ZC3H14, PGAP1, EDC3, NAA15, RAB11B, TECR, KYNU, NDP, MAPT, MECP2, MEFV, MGAT2, MITF, KMT2A, NTRK2, SARS1, OCRL, PPP2R1A, PPP3CA, PRODH, PSEN1, RAC1, LETM1, NDST1, HNMT, GRIK2, GRN, GABRD, FLII, FOXG1, FGFR2, EXT2, EP300, DNM1, DDX3X, CTBP1, CREBBP, CHD3, CHD1, CLIP1, PIGC, SCN8A, SMC1A, TRIO, TKT, VCP, EZR, WHCR, TCF4, TBCD, NSD2, TUSC3, TBX1, SYT1, CDKL5, SOX5, SNRPN, NAA10, SLC6A8, PRSS12, KCNAB2, CRADD, SKI, SYNGAP1, ST3GAL3, ST3GAL5, SQSTM1, IGH, IGHV3OR16-7, LOC102723407, IGHV3-69-1, LOC102724971, CDR3, IGHD, SLC1A1, SLC6A3, IGLV@, STX2, IGHV4-34, IGHV3-21, IGLL5, LOC390714, BCR, CHAT, IGHV1-69, REM1, RGS4, RELN, DRD1, SNCA, WASF1, IL13, UBR4, PRTFDC1, MET, TH, GAD1, BMS1P20, GDNF, GFAP, MAP6, NOD2, GRIN1, HMOX1, LAIR1, TP53, LOC105379528
- Stereotypic Movement Disorder Wikipedia
  
  Not to be confused with Stereotypy . Stereotypic movement disorder Specialty Psychiatry Stereotypic movement disorder ( SMD ) is a motor disorder with onset in childhood involving repetitive, nonfunctional motor behavior (e.g., hand waving or head banging), that markedly interferes with normal activities or results in bodily injury. [1] To be classified as SMD, the behavior in question must not be due to the direct effects of a substance or another medical condition. [1] The cause of this disorder is not known. [2] Contents 1 Signs and symptoms 2 Diagnosis 2.1 Classification 2.2 Differential diagnosis 3 Treatment 4 Prognosis 5 Epidemiology 6 References 7 Further reading 8 External links Signs and symptoms [ edit ] Common repetitive movements of SMD include head banging, arm waving, hand shaking, rocking and rhythmic movements, self-biting, self-hitting, and skin-picking; [1] other stereotypies are thumb-sucking, nail biting, trichotillomania , bruxism and abnormal running or skipping. [3] Diagnosis [ edit ] Stereotyped movements are common in infants and young children; if the child is not distressed by movements and daily activities are not impaired, diagnosis is not warranted. [1] When stereotyped behaviors cause significant impairment in functioning, an evaluation for stereotypic movement disorder is warranted. There are no specific tests for diagnosing this disorder, although some tests may be ordered to rule out other conditions. SMD may occur with Lesch–Nyhan syndrome , intellectual disability, and fetal alcohol exposure or as a result of amphetamine intoxication. [1] When diagnosing stereotypic movement disorder, DSM-5 calls for specification of: with or without self-injurious behavior ; association with another known medical condition or environmental factor; severity (mild, moderate or severe). [1] Classification [ edit ] Stereotypic movement disorder is classified in the fifth revision of the Diagnostic and Statistical Manual of Mental Disorders ( DSM-5 ) as a motor disorder , in the category of neurodevelopmental disorders . [1] Differential diagnosis [ edit ] Other conditions which feature repetitive behaviors in the differential diagnosis include autism spectrum disorders , obsessive–compulsive disorder , tic disorders (e.g., Tourette syndrome ), and other conditions including dyskinesias . [1] Stereotypic movement disorder is often misdiagnosed as tics or Tourette syndrome (TS). [4] [5] Unlike the tics of TS, which tend to appear around age six or seven, repetitive movements typically start before age three, [1] [6] are more bilateral than tics, and consist of intense patterns of movement for longer runs than tics. Tics are less likely to be stimulated by excitement. Children with stereotypic movement disorder do not always report being bothered by the movements as a child with tics might. [4] [6] Treatment [ edit ] There is no consistently effective medication for SMD, and there is little evidence for any effective treatment. [4] In non-autistic habit reversal training may be useful [4] as well as decoupling . [7] No treatment is an option when movements are not interfering with daily life. [3] Prognosis [ edit ] Prognosis depends on the severity of the disorder. Recognizing symptoms early can help reduce the risk of self-injury, which can be lessened with medications.
Propionic Acidemia Wikipedia

.; Ferry, Susan; Pass, Alexandra; Van Ryzin, Carol; Myles, Jennifer; Schoenfeld, Megan; McGuire, Peter; Rosing, Douglas R.; Levin, Mark D. (2019-06-28). "Chronic kidney disease in propionic acidemia" .
Social Communication Disorder Wikipedia

. ^ "Social (Pragmatic) Communication Disorder" (PDF) . Retrieved September 28, 2013 . ^ Mash, Eric. (2016). Abnormal Child Psychology, 6e, 6th Edition .

GABRA5, UCHL1, ADNP, DNAJC6, MED12, TUBB3, TBR1, PARK7, IQSEC2, CNTNAP2, SNCA, HTRA2, VPS13C, PINK1, LRRK2, HGSNAT, NRXN1, ALG11, PRKN, SLC6A8, PTEN, PODXL, KMT2A, SHANK3, NLGN3, SLC9A9, CTSS, EN2, CAPS2, MECP2, TNF, NTF3, TSC1, PIK3CA, PIK3CB, PIK3CD, PIK3CG, SMARCA2, CRH, BDNF
- Social (Pragmatic) Communication Disorder Wikipedia
  
  Social (pragmatic) communication disorder Other names SPCD Specialty Speech pathology Social (pragmatic) communication disorder (SPCD) is a disorder where individuals have difficulties with verbal and nonverbal social communication. [1] As well, SPCD lacks behaviors associated with restrictions and repetition. [2] Relates to Pragmatic Language Impairment and Autism Spectrum Disorder . It has only been within the last six years (in 2013) that SPCD has become its own category in the DSM-5 . [3] In creating this new category it allowed individuals to be considered with a form of disorder that was different from PLI and ASD. [4] Contents 1 Presentation 2 Diagnosis 3 History 4 References Presentation [ edit ] Issues with communication for social purposes Unable to adapt communication to context Struggles to follow conversation and story type situation Unable to understand abstract ideas. [3] Diagnosis [ edit ] Due to the fact that the SPCD has only been categorized in the last six years, diagnosis is yet to be fully established. In the DSM-5 , the child is diagnosed with SCD if the child does not meet the criteria for other disorders such as ASD and PDD-NOS . [3] Common assessments used to identify SPCD are: The developmental, dimensional and diagnostic interview (3Di) [5] The child communication checklist (CCC) [5] The strengths and difficulties questionnaire (SDQ) [5] Natural Observation Targeted Observation of Pragmatics in Children's Conversations (TOPICC) [5] Analysis of Language Impaired Children's Conversation (ALICC) [5] Structured Observation [5] Test of Language Competence [5] Assessment of Comprehension and Expression (ACE 6‐11) [5] Test of Pragmatic Language [5] Bus story [5] Expression, Reception and Recall of Narrative Instrument (ERRNI) [5] Although there are several tests that can be done to try to identify SPCD, there are some tests that are better suited to diagnose SPCD than others. As well, there is not a specific assessment or test that is able to diagnose SPCD unlike other disorders such as ASD, DLD and PLI. History [ edit ] As mentioned in the introduction, SPCD has only been around for the last six years.
Endophthalmitis Wikipedia

"Bacterial contamination of ocular surface and needles in patients undergoing intravitreal injections". Retina (Philadelphia, Pa.) . 28 (6): 877–883. doi : 10.1097/IAE.0b013e31816b3180 .

TNF, FAS, IFNG, IL1B, SLPI, VEGFA, PRF1, TLR4, TLR2, CCL18, MYD88, HMGB1, INSRR, IL10, IL6, PER2, EFS, CUL9, NTM, CARD9, TRIM69, TICAM1
- Ophthalmia Wikipedia
  
  "Ophthalmitis" redirects here. For the genus of geometer moth, see Ophthalmitis (moth) . Ophthalmia (also called ophthalmitis ) is inflammation of the eye. It is a medical sign which may be indicative of various conditions, including sympathetic ophthalmia (inflammation of both eyes following trauma to one eye), gonococcal ophthalmia, trachoma or " Egyptian " ophthalmia, ophthalmia neonatorum (a conjunctivitis [1] of the newborn due to either of the two previous pathogens), photophthalmia and actinic conjunctivitis (inflammation resulting from prolonged exposure to ultraviolet rays), and others. Noted historical sufferers [ edit ] Aristodemus, a Spartan captain during the Second Persian invasion of Greece , was afflicted with ophthalmia and was thus unable to fight at the Battle of Thermopylae (of the famous Spartan 300). However, he fought bravely and died at the Battle of Plataea . Due to the ophthalmia, and his absence from the first battle, he was not buried with proper funeral rites of a Spartan captain. [2] Cicero, on 1 March 49 BC wrote to Atticus that he was suffering from ophthalmia. [3] Eratosthenes , who among other things was a Greek geographer and mathematician, contracted ophthalmia as he aged, becoming blind around 195 BC, depressing him and causing him to voluntarily starve himself to death. He died in 194 BC at the age of 82. [4] Hannibal 's sight was lost in his right eye in 217 BC by what was likely ophthalmia.
- Endophthalmitis Orphanet
  
  A rare ophthalmic disorder characterized by inflammation involving the vitreous and/or aqueous humors, usually due to bacterial or fungal infection. It may arise endogenously from hematogenous spread of the infectious agent, or exogenously after direct inoculation, and can take an acute or chronic course. Clinical signs and symptoms include progressive vitritis, hypopyon, reduced or blurred vision, red eye, pain, and lid swelling. The condition may be complicated by panophthalmitis, corneal infiltration and perforation, affection of orbital structures, and phthisis bulbi.
Palinopsia Wikipedia

Brain : A Journal of Neurology . 131 (Pt 3): 818–28. doi : 10.1093/brain/awn007 . PMID 18238797 . ^ Purvin, V; Bonnin, J; Goodman, J (Dec 1989).
Cyclosporiasis Wikipedia

Journal of Nepal Health Research Council. 2008; 6(12): 28–37. https://www.nepjol.info/index.php/JNHRC/article/download/2441/2177 ^ "Surveillance for Laboratory-Confirmed Sporadic Cases of Cyclosporiasis --- United States, 1997--2008" . cdc.gov . ^ "Case Count Maps - Outbreak Investigations 2013 - Cyclosporiasis - CDC" . cdc.gov . 2019-04-12. ^ "CDC: 425 cases of cyclospora infection identified across 16 states" . cbsnews.com . 5 August 2013. ^ http://www.idph.state.ia.us/IDPHChannelsService/file.ashx?
Pathological Lying Wikipedia

. ^ "The Truth About Compulsive and Pathological Liars" . Psychologia . Retrieved 28 January 2017 . ^ a b c d e King BH, Ford CV (January 1988).
Mansonelliasis Wikipedia

Adult worms recovered from experimentally infected Patas monkeys measured 24 to 28 mm long and 70 to 80 μm in diameter (males) and 32 to 62 mm long and .130 to .160 mm in diameter (females). [1] Adults produce unsheathed and non-periodic (sub-periodic in M. perstans ) microfilariae that reach the blood stream.

CXCL10, CXCL9, CCL13, CCL17, CCL18, CCL22, CCL24, IL17D, MYDGF, IL27
- Mansonelliasis Orphanet
  
  Mansonellosis is a mild form of filariasis (see this term), distributed throughout sub-Saharan Africa as well as in some locations of Central and South America and the Caribbean, caused by the parasitic worms Mansonella perstans and Mansonella ozzardi . The disease is often asymptomatic but may also cause fever, vertigo, myalgias, arthralgias and a sensation of coldness in the legs. Additional features include neuropsychiatric symptoms, skin rash, pruritus, nodules containing adult worms (in the conjunctiva or eyelids), lymphadenopathy, recurrent lymphedema in the limbs and face (resembling the Calabar swellings of loasis (see this term)), severe abdominal pain and endocrine disturbances.
Occupational Hazards Of Human Nail Dust Wikipedia

The resulting treatment for mycosis improved the patient's asthmatic condition. [24] The antifungal treatment of many other trichophyton foot infections has alleviated symptoms of hypersensitivity, asthma, and rhinitis. [1] [23] [24] [25] [26] [27] [28] Control measures [ edit ] Chronic exposure to human nail dust is a serious occupational hazard that can be minimized by not producing such dust.
Poikiloderma Vasculare Atrophicans Wikipedia

. ^ a b "A definition of the term "poikiloderma" from Medterms.com" . Retrieved Dec 28, 2009 . ^ Brocq L (1902). "Les parapsoriasis".
- Retiform Parapsoriasis Wikipedia
  
  Retiform parapsoriasis Specialty Dermatology Retiform parapsoriasis is a cutaneous condition, considered to be a type of large-plaque parapsoriasis . [1] It is characterized by widespread, ill-defined plaques on the skin, that have a net-like or zebra-striped pattern. [2] Skin atrophy , a wasting away of the cutaneous tissue , usually occurs within the area of these plaques. [1] See also [ edit ] Parapsoriasis Poikiloderma vasculare atrophicans List of cutaneous conditions References [ edit ] ^ a b Lambert WC, Everett MA (Oct 1981). "The nosology of parapsoriasis". J. Am. Acad. Dermatol . 5 (4): 373–95. doi : 10.1016/S0190-9622(81)70100-2 . PMID 7026622 . ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set . St. Louis: Mosby. ISBN 1-4160-2999-0 . External links [ edit ] Classification D ICD - 10 : L41.5 ICD - 9-CM : 696.2 v t e Papulosquamous disorders Psoriasis Pustular Generalized pustular psoriasis ( Impetigo herpetiformis ) Acropustulosis / Pustulosis palmaris et plantaris ( Pustular bacterid ) Annular pustular psoriasis Localized pustular psoriasis Other Guttate psoriasis Psoriatic arthritis Psoriatic erythroderma Drug-induced psoriasis Inverse psoriasis Napkin psoriasis Seborrheic-like psoriasis Parapsoriasis Pityriasis lichenoides ( Pityriasis lichenoides et varioliformis acuta , Pityriasis lichenoides chronica ) Lymphomatoid papulosis Small plaque parapsoriasis ( Digitate dermatosis , Xanthoerythrodermia perstans ) Large plaque parapsoriasis ( Retiform parapsoriasis ) Other pityriasis Pityriasis rosea Pityriasis rubra pilaris Pityriasis rotunda Pityriasis amiantacea Other lichenoid Lichen planus configuration Annular Linear morphology Hypertrophic Atrophic Bullous Ulcerative Actinic Pigmented site Mucosal Nails Peno-ginival Vulvovaginal overlap synromes with lichen sclerosus with lupus erythematosis other: Hepatitis-associated lichen planus Lichen planus pemphigoides Other Lichen nitidus Lichen striatus Lichen ruber moniliformis Gianotti–Crosti syndrome Erythema dyschromicum perstans Idiopathic eruptive macular pigmentation Keratosis lichenoides chronica Kraurosis vulvae Lichen sclerosus Lichenoid dermatitis Lichenoid reaction of graft-versus-host disease This dermatology article is a stub . You can help Wikipedia by expanding it . v t e
Perineal Tear Wikipedia

Women and Birth : Journal of the Australian College of Midwives . 28 (3): 194–8. doi : 10.1016/j.wombi.2015.02.006 .
Papillary Tumors Of The Pineal Region Wikipedia

Papillary tumor of the pineal region. Neuropathology, 28, 87-92. ^ a b c d e f g Katherine Poulgrain, R.

BRAF, CRX, FOXJ1, IDH1, SPDEF
- Papillary Tumor Of The Pineal Region Orphanet
  
  Papillary tumor of the pineal region (PTPR) is a very rare neoplasm of the pineal region that is thought to arise from the specialized ependymocytes of the subcommissural organ and that manifests with visual disturbances, headaches, loss of coordination and balance, nausea and vomiting due to obstructive hydrocephalus.