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Pallor Mortis Wikipedia

After-death paleness that occurs in those with light/white skin Stages of death Pallor mortis Algor mortis Rigor mortis Livor mortis Putrefaction Decomposition Skeletonization Fossilization v t e Pallor mortis ( Latin : pallor "paleness", mortis "of death"), the first stage of death , is an after-death paleness that occurs in those with light/white skin. [1] An opto-electronical colour measurement device is used to measure pallor mortis on bodies. [2] Timing and applicability [ edit ] Pallor mortis occurs almost immediately, generally within 15–25 minutes, after death.
Systemic-Onset Juvenile Idiopathic Arthritis Orphanet

Management and treatment Management by a specialized multidisciplinary team is required. Treatment is typically first with non-steroidal anti-inflammatory drugs (NSAIDs) and, if the inflammation is not controlled, followed by high dose corticosteroids.

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- Rheumatoid Arthritis, Systemic Juvenile Omim
  
  A number sign (#) is used with this entry because multiple factors influence the susceptibility to systemic juvenile rheumatoid arthritis. Polymorphisms in the IL6 (147620.0001) and in the MIF gene (153620.0001) have been found to be associated with susceptibility to the disorder. Glass and Giannini (1999) reviewed juvenile rheumatoid arthritis as a complex genetic trait. Clinical Features Systemic juvenile rheumatoid arthritis is a subset of juvenile chronic, or idiopathic, arthritis, representing approximately 11% of patients with this disease. The systemic-onset form represents a subgroup most likely to be associated with severe, debilitating, extraarticular features, and occasionally fatal complications.
- Systemic-Onset Juvenile Idiopathic Arthritis Wikipedia
  
  The rash is commonly seen on trunk and proximal extremities or over pressure areas. [ citation needed ] Arthritis is often absent in the first weeks or even 6–8 months into the illness.Systemic JIA may have internal organ involvement such as hepatosplenomegaly, lymphadenopathy, serositis , hepatitis , or tenosynovitis . [ citation needed ] A polymorphism in macrophage migration inhibitory factor has been associated with this condition. [3] Cause [ edit ] The cause is unknown but it's thought to be related to environmental, genetic, and hormonal factors. [ citation needed ] Diagnosis [ edit ] Rheumatoid factor and ANA tests are generally negative in systemic JIA.
Atonic Seizure Wikipedia

As with common epileptic occurrences, no first aid is needed post-seizure, except in the instances where falling injuries have occurred.

SLC6A1, HCN1, PIGM, GAMT, MECP2, CDKL5, PNKP, POMC, PDYN, POLG, PTGS2, PRKCD, OXT, PVALB, REST, SLC1A1, PAM, ABAT, OPRM1, OPRK1, SLC2A1, NOS2, NOS1, NGFR, NGF, MT3, LETM1, LEP, KCNQ2, ACAT1, SLC8A1, SLC6A2, KCNA2, MIB1, SLC12A5, SLC17A7, PLPPR1, CNNM2, RBFOX1, GHRL, SIGMAR1, NRP2, MPDZ, SLC30A1, TSC2, TSC1, TRH, TCF4, TBCD, SYN2, SSTR2, SST, SOD2, SLC8A3, KCNJ11, NPY, ADORA2A, CHAT, FGF2, FAAH, DRD3, ALAD, ATP7A, CCK, DRD2, DRD1, ADRA1B, CYP11A1, CRH, CNR1, ABCC2, CLU, CHRNB4, CHRNA7, INS, CHRNA5, CHRNA4, CHRNA3, AGT, ALPL, FOXG1, CAT, FOS, IMPA1, BCHE, IL6, IL1B, IFNB1, IDH2, HTR1B, ACHE, HTR1A, GRIK1, GNB3, GAD2, APOE, APEX1, BDNF, GABRA5, ADCYAP1, CHRM1, ABCB1, SCN1A, PIGP, PHGDH, KCNA1, NGLY1, PCDH19, SLC25A22, TRIM8, ADGRV1, STX1B, PRICKLE1, SIK1, ARX, NHLRC1, ST20-MTHFS, CUX2, STXBP1, MTHFS, SCN2A, KCNMA1, NEUROD2, GNAO1, GABRG2, GABRD, GABRB3, GABRA1, MAPK10, ATP6AP2, SCN1B, SCN9A, DNM1, CHD2, EPM2A, CASK, PIGQ, GOSR2, KCNMA1-AS1, FOLR1, TK2, SYNGAP1, TRNK
Chvostek Sign Wikipedia

In his professional life, Chvostek devoted himself to the study of etiopathogenesis and to the treatment of neurological disorders, including by means of electrotherapy. In 1876, he first described the sign that bears his name. [2] Later it was independently described by another Austrian physician, Nathan Weiss (1851–1883), in 1883. [3] Features [ edit ] Chvostek sign – type I [ edit ] It is obtained by striking with a finger or a hammer a point that is approximately 2 cm in front of the lobe of the ear and about 1 cm below the zygomatic process .
Hyperthecosis Wikipedia

Women with hyperthecosis have a significant degree of insulin resistance and insulin may stimulate the ovarian stromal androgen synthesis. [8] Prognosis [ edit ] Although no large studies showing the long term outcomes for women with hyperthecosis exist, a diagnosis of hyperthecosis may suggest an increased risk for metabolic complications of hyperlipidemia and type 2 diabetes . [9] In postmenopausal women, hyperthecosis may also contribute to the pathogenesis of endometrial polyp, endometrial hyperplasia, and endometrioid adenocarcinoma due to the association of hyperestrinism (excess estrins in the body) and hyperthecosis. [10] Treatment for hyperthecosis is based upon each case, but may range from pharmacological interventions to surgical. [11] See also [ edit ] Polycystic ovary syndrome References [ edit ] ^ Taber's Cyclopedic Medical Dictionary 21st Edition ^ Stead, Stead, Kaufman, Suarez (2009). First Aid for the Obstretrics & Gynecology Clerkship - Second Edition.
Trevor Disease Wikipedia

Synovial chondromatosis occurs in a much older age group and can be ruled out on this basis. [2] Treatment [ edit ] Most reported cases of DEH in the literature have been treated surgically, usually with excision of the mass, as well as by the correction of any deformity, while preserving the integrity of the affected joint as much as possible. [2] [11] [12] [13] History [ edit ] Trevor disease was first described by the French surgeon Albert Mouchet and J.

EXT1, IHH
- Dysplasia Epiphysealis Hemimelica Gard
  
  Dysplasia epiphysealis hemimelica (DEH), or Trevor's disease, is a rare condition that most commonly affects the epiphysis (the end) of long bones in children. Early diagnosis and treatment are necessary to prevent joint dysfunction and deformity and may be surgical or non-surgical depending on the location and the symptoms. Due to the progressive nature of this disorder and the chance of worsening deformity, patients should be followed until skeletal maturity. The cause of dysplasia epiphysealis hemimelica is not known.
- Dysplasia Epiphysealis Hemimelica Omim
  
  This condition is characterized by asymmetrical cartilaginous overgrowth of one or more epiphyses of a tarsal or carpal bone, and less often other bones. Males are affected about 3 times more often than females. The disorder appears to have no simple mendelian basis. No familial case has been reported. Donalson et al. (1953) described a patient whose monozygotic twin was not affected. Wiedemann et al. (1981) described a case with involvement of both legs and, to a lesser extent, of the arms, and suggested that this is a systemic disorder. It is likely that the familial disorder described in 127820 is a separate entity.
- Dysplasia Epiphysealis Hemimelica Orphanet
  
  A rare bone development disorder characterized by localized, asymmetric osteochondral overgrowth affecting single or multiple epiphyses, most commonly the distal femur, proximal tibia, and talus. The lesions are typically restricted to one side of the epiphysis, with the medial side being affected twice as often as the lateral side. The condition is usually diagnosed in children, and three times more often in boys than in girls. Patients present with pain, limitation in range of motion, and deformity or swelling of the affected joint.
Methylmalonic Aciduria, Cbla Type Omim

Most cblA, cblB, and mut(-) patients were still living at the time of the report; most mut(0) patients died during the first few months of life. Dobson et al. (2002) confirmed the cblA phenotype by molecular analysis in 4 patients with MMA.

MMAA
- Vitamin B12-Responsive Methylmalonic Acidemia Orphanet
  
  An inborn error of vitamin B12 (cobalamin) metabolism characterized by recurrent ketoacidotic comas or transient vomiting, dehydration, hypotonia and intellectual deficit, which responds to vitamin B12. There are three types: cblA, cblB and cblD -variant 2 ( cblD v2). Epidemiology To date, over 120 patients with cblA , 66 patients with cblB and 6 patients with cblD v2 have been reported. Prevalence of 1/48,000-1/61,000 have been reported for methylmalonic acidemia (MA) of all causes in North America, and 1/26,000 in China, but only a subset of this is vitamin B12-responsive MA. Clinical description Patients usually present in infancy or early childhood with features including lethargy, failure to thrive, recurrent vomiting, dehydration, respiratory distress, muscle hypotonia, hepatomegaly and coma. They may also show signs of anemia (not megaloblastic), have potentially life-threatening ketoacidosis and/or hyperammonemia, and developmental delay and intellectual deficit, with metabolic stroke affecting the brain stem.
Ramsay Hunt Syndrome Type 1 Wikipedia

You can help by adding to it . ( February 2017 ) Treatment [ edit ] Treatment of Ramsay Hunt Syndrome Type 1 is specific to individual symptoms. [1] Myoclonus and seizures may be treated with drugs like valproate . [1] Some have described this condition as difficult to characterize. [7] Eponym [ edit ] It is named for James Ramsay Hunt [8] who first described a form of progressive cerebellar dyssynergia associated with myoclonic epilepsy in 1921. [1] References [ edit ] ^ a b c d e f g h i "National Institute of Neurological Disorders and Stroke" .
- Cerebelloparenchymal Disorder V Omim
  
  Ramsey Hunt (1921) described twin brothers with a cerebellar disturbance combined with severe myoclonic jerks brought on by muscular effort. Autopsy in one of them who died at age 36 years showed marked loss of dentate neurons and their fibers in the superior cerebellar peduncles. Hunt described several other cases with affected relatives and without autopsy. Neuro - Ataxia - Myoclonic jerks Lab - Dentate neuron loss - Superior cerebellar peduncle fiber loss Inheritance - Autosomal recessive ▲ Close
Phlebitis Wikipedia

Symptoms may be worse when the leg is lowered, especially when first getting out of bed in the morning.
Acne Cosmetica Wikipedia

People may not attribute skin reactions to their cosmetics at first, but may notice worsening symptoms after using certain face makeup , sunblock or lip products.
Severe Fever With Thrombocytopenia Syndrome Wikipedia

Severe fever with thrombocytopenia syndrome SFTS bunyavirus isolated from patients in Central and Northeast provinces of China (red) Specialty Infectious disease Severe fever with thrombocytopenia syndrome ( SFTS ) is an emerging infectious disease caused by Dabie bandavirus also known as the SFTS virus , first reported between late March and mid-July 2009 in rural areas of Hubei and Henan provinces in Central China. [1] SFTS has fatality rates ranging from 12% to as high as 30% in some areas.

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Hysterotomy Abortion Wikipedia

Hysterotomy abortion Background Abortion type Surgical First use <1913 Gestation 2nd Trimester and Later Usage U.S. figures include both hysterotomy and hysterectomy .
Susto Wikipedia

Retrieved 6 March 2013 . v t e Superstition Main topics Amulet Evil eye Luck Omen Talismans Myth and ritual Lists List of superstitions List of lucky symbols List of bad luck signs Sailors' superstitions Theatrical superstitions Africa Buda Gris-gris Sampy Sleeping child Americas Ascalapha odorata Carranca Cooties Curupira Djucu Fortune cookie Groundhog Day I'noGo tied Oscar love curse Susto White lighter myth Witch window Asia Superstition in India Superstition in Pakistan Japanese superstitions Bhoot (ghost) Chhaupadi Churel Ghosts in Bengali culture Jackal's horn Kuai Kuai culture Muhurta Navaratna Nazar battu Pichal Peri Puppy pregnancy syndrome Akabeko Kanai Anzen Maneki-neko Okiagari-koboshi Omamori Fan death Agimat Arbularyo Barang Kulam Lihi Pagtatawas Pasma Usog Kuman Thong Palad khik Takrut Nang Kwak White elephant Curse of 39 Jin Chan Numbers in Chinese culture Superstitions of Malaysian Chinese Europe August curse Barbary macaques in Gibraltar Bayern-luck Blarney Stone Cimaruta Cornicello The Goodman's Croft Himmelsbrief Icelandic magical staves In bocca al lupo Kitchen witch Klabautermann Mooncalf Nazar Need-fire Painted pebbles Powder of sympathy Rabbit rabbit rabbit Ravens of the Tower of London Russian traditions and superstitions Spilling water for luck The Scottish Play Troll cross Tycho Brahe days Witch post Wolfssegen General 11:11 4 ( Four-leaf clover , Tetraphobia ) 7 ( Seventh son of a seventh son ) 8 9 13 ( Friday the 13th , The Thirteen Club , Thirteenth floor , Triskaidekaphobia ) 108 111 666 ( Number of the Beast ) Ace of spades Auspicious wedding dates Baseball superstition Beginner's luck Black cat Bread and butter Break a leg Chain letter Cramp-ring Curse Davy Jones' Locker Dead man's hand End-of-the-day betting effect Fear of frogs Fear of ghosts First-foot Flying Dutchman Four Eleven Forty Four Gambler's conceit Good luck charm Human sacrifice Jinx Knocking on wood Law of contagion Literomancy Lock of hair Maternal impression Miasma theory Nelson Numismatic charm Penny Rabbit's foot Rainmaking Ship sponsor Shoes on a table Sign of the horns Something old Spilling salt Statue rubbing Three on a match Threshold Toi toi toi 27 Club Wishing well Witch ball Witching hour Related Apotropaic magic Astrology and science Coincidence Debunker Divination Folk religion Fortune-telling Magic and religion Magical thinking Numerology Perceptions of religious imagery in natural phenomena Post hoc ergo propter hoc Traditional medicine Urban legend Jew Muslim
Abortion In Qatar Wikipedia

Furthermore, a law formalized in 1983 states that abortions may be legally performed on pregnancies of less than four months duration if the pregnancy were to cause serious harm to the mother's health if continued, or if there was evidence that the child would be born with untreatable mental or physical deficiencies and both parents consented to the abortion. [1] Abortions must first be recommended by a medical commission comprising three specialists before it can be performed.
Abortion In Nauru Wikipedia

. ^ a b c d Hall, Bianca (2016-05-11). "First she was raped on Nauru. Now 'S99' is trapped in another nightmare" .
Pseudocholinesterase Deficiency Mayo_clinic

Risk factors Your risk of having pseudocholinesterase deficiency is higher if you or a first-degree relative, such as a parent, child or sibling, has: A gene change that causes the disorder A history of a problem during anesthesia that is suspected to be caused by pseudocholinesterase deficiency Prevention If you have a family history of pseudocholinesterase deficiency or have a family member who had any problem with anesthesia, tell your health care provider before getting a medical procedure that requires anesthesia.

BCHE, COLQ
Trifascicular Block Wikipedia

Finally, the third meaning of trifascicular block refers to a specific finding on an electrocardiogram in which bifascicular block is observed in a patient with a prolonged PR interval ( first degree AV block ). The treatment of trifascicular block is highly dependent on which clinical entity (one of the three above) is being described.

CACNA1C, SCN10A, TRPM4, RANGRF, KCNE5, GPD1L, AKAP9, ABCC9, HCN4, KCNE3, SLMAP, SCN5A, CACNA2D1, SCN2B, SCN1B, PKP2, KCNJ8, KCND3, CALM2, CACNB2, SCN3B, POMC, LCT
Respiratory Distress Syndrome In Premature Infants Omim

The association was particularly apparent in first-born male infants. Marttila et al. (2003) stated that the traditional twin concordance study appeared insufficient to evaluate genetic predisposition to RDS or other disorders that are confounded by birth order or multiple pregnancy.

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Emergence Delirium Wikipedia

Anaesth. (2014) doi: 10.1093/bja/aeu442 First published online: December 23, 2014 Further reading [ edit ] Vlajkovic GP, Sindjelic RP (Jan 2007).

ARSA, BCHE
Flatfeet Mayo_clinic

Before the appointment, you might want to write answers to the following questions: When did you first notice problems with your feet?

HOXD10, ELN, AUTS2, B4GALT7, EXOC6B, PHF8, IQSEC2, DHX30, CNKSR2, PUF60, AP4S1, ADNP, IL1RAPL1, PRDM5, MID2, TLK2, RAI1, STAG2, MED13L, AP4E1, RIN2, ATP6V0A2, FLRT3, FTSJ1, RAB3GAP2, NSMF, B3GAT3, BSCL2, TBL2, UBE2T, ANKRD11, GMPPB, ZDHHC9, RLIM, DACT1, AP4B1, ABL1, DEAF1, CCNK, AP4M1, AIFM1, BAZ1B, HERC1, FGF17, HESX1, CDK10, TRIP4, OFD1, CUL4B, USP9X, GDF5, GAN, MFAP5, CRLF1, EFTUD2, SEC23A, AMMECR1, MAD2L2, SEMA3A, ATP6AP2, HUWE1, SCO2, MED12, CUL7, LONP1, FRMPD4, GTF2IRD1, TBX4, CHST3, ARHGEF6, HS6ST1, DPM3, IL17RD, ALMS1, SLC9A7, C12orf57, STX1B, GORAB, RFT1, SLC39A13, ALG2, MYPN, CANT1, KISS1R, ZNF469, SLX4, ADGRV1, BRIP1, SPRTN, RAB39B, B3GALT6, PHIP, CCDC141, GDF6, USP27X, FEZF1, PTPRQ, HCN1, ZNF81, BRWD3, PROKR2, ALG14, ARX, VPS13B, PTCHD1, NDUFAF6, TANGO2, RAB33B, LAS1L, SPRY4, IARS2, FANCM, CHD8, SELENON, SALL4, HDAC8, WDR11, PACS1, TRIM8, CHD7, SLC29A3, FANCI, RFWD3, FANCL, FKBP14, WDR19, TRPV4, PROK2, PIEZO2, CXorf56, XYLT1, XYLT2, NSD1, SIL1, REEP1, UPF3B, PALB2, EHMT1, ALG13, PYROXD1, FBXO11, ASXL3, RAB7A, ZNF148, ACTA2, BPTF, FGF8, FGD1, FBN1, FANCG, FANCF, FANCB, ACSL4, FOXG1, FANCE, FANCD2, FANCC, FANCA, EXT2, ERCC4, FGFR1, FOXE3, GRM1, GABRG2, GRIA3, GLI3, GFPT1, GDI1, GATA4, GARS1, GABRD, FLI1, MTOR, FN1, FMR1, FLNB, FLNA, FLII, EP300, DUSP6, DPAGT1, ATR, CAPN1, CACNA1A, BRCA2, BRCA1, BCR, ATRX, ATP7A, DMD, ATP6V1E1, ATP6V1B2, AHCY, AGTR2, AGA, AEBP1, CTSC, CHAT, CLCN4, COL1A1, COL1A2, COL2A1, COL5A1, COL5A2, COL6A1, COL6A2, COL6A3, COL12A1, CPT2, CREBBP, CRKL, DCC, DLG3, GRIN2D, GTF2I, ZNF41, SCN2A, TACR3, SYP, SOX10, SLC16A2, SKI, SCN9A, SCN1B, TGFB1, SCN1A, SBF1, SARS1, SALL1, RYR1, RPS6KA3, TCF4, TGFB2, HCFC1, TTN, ZNF711, XRCC2, CLIP2, VLDLR, UCHL1, UBE2A, TRPS1, TGFB3, TRIO, TPM3, TPM2, TSPAN7, TGFBR2, TGFBR1, RFC2, CHCHD10, RAD51C, LMNA, MGAT2, MECP2, MAT2A, SMAD3, LOX, LMX1B, LIMK1, RAD51, LIFR, KIF22, KCNH1, ANOS1, HSPG2, HNRNPH2, MMP2, MYH7, MYH11, MYLK, NONO, PAK3, CHMP1A, PEX1, PEX6, PLOD1, PMM2, PRKG1, MAPK1, PTCH1, PURA, PYCR1, ALDH18A1, PDPN
- Flat Feet Wikipedia
  
  Weight-bearing lateral X-ray showing the measurement of calcaneal pitch , which is an angle of the calcaneus and the inferior aspect of the foot, with different sources giving different reference points. [12] A calcaneal pitch of less than 17° or 18° indicates flat feet. [10] Same lateral X-ray showing the measurement of Meary's angle, which is the angle between the long axis of the talus and first metatarsal bone . [10] An angle greater than 4° convex downward is considered a flat foot, 15° - 30° moderate flat foot, and greater than 30° severe flat foot. [10] Treatment [ edit ] Most flexible flat feet are asymptomatic, and do not cause pain.