Cach Syndrome

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Retrieved

2021-01-23

Source

Orphanet

Trials

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Genes

EIF2B5, EIF2B4, EIF2B1, EIF2B2, EIF2B3, MTHFR, MTR, RHOA, SCP2, TCN2, DPYD, SPP1, CSF1R, COL4A1, EIF2S2, EIF2S1, TNF, IFNA1, IFNA13, ACOT12, EIF2S3, TRIM21, IL6, TNFRSF12A, HMGB1, SIGMAR1, TREX1, CHST11, TIMP1, RTRAF, TLR9, SOCS1, TRIM39, IFNK, TLR4, RPP21, TRIM39-RPP21, APRT, PITX1, SOS1, SOAT1, ATF4, TNFRSF8, DEFB1, DNASE1, HAS2, HLA-DQA1, HSPA4, IFNG, IL17A, CXCL10, MFAP1, MICB, MMP2, MMP9, MSH5, RASGRF1, S100A7, MICA

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A new leukoencephalopathy, the CACH syndrome (Childhood Ataxia with Central nervous system Hypomyelination) or VWM (Vanishing White Matter) was identified on clinical and MRI criteria. Classically, this disease is characterized by (1) an onset between 2 and 5 years of age, with a cerebello-spastic syndrome exacerbated by episodes of fever or head trauma leading to death after 5 to 10 years of disease evolution, (2) a diffuse involvement of the white matter on cerebral MRI with a CSF-like signal intensity (cavitation), (3) a recessive autosomal mode of inheritance, (4) neuropathologic findings consistent with a cavitating orthochromatic leukodystrophy with increased number of oligodendrocytes with sometimes ``foamy'' aspect.

Epidemiology

A total of 148 cases have been reported so far. Prevalence of this disease remains unknown.

Clinical description

Clinical symptoms are variable, from fatal infantile forms (Cree leukoencephalopathy) and congenital forms associated with extra-neurological affections, to juvenile and adult forms (ovarioleukodystrophy) characterized by cognitive and behavioural dysfunctions and by a slow progression of the disease, leading to the term of eIF2B-related leukoencephalopathies.

Etiology

This disease is linked to mutations in the five EIF2B genes encoding the five subunits of the eukaryotic initiation factor 2B (eIF2B), involved in the protein synthesis and its regulation under cellular stress. The patho-physiology of the disease would involve a deficiency in astrocytes maturation leading to an increased susceptibility of the white matter to cellular stress.

Diagnostic methods

Diagnosis relies on the detection of eIF2B mutations, predominantly affecting the EIF2B5 gene. A decrease in the intrinsic activity of the eIF2B factor (the guanine exchange activity, GEF) in lymphoblasts from patients seems to have a diagnostic value.

Management and treatment

No specific treatment exists besides the ``prevention'' of cellular stress. Corticosteroids sometimes proved to be useful in acute phases.

Prognosis

Prognosis seems to be correlated with the age of onset, the earliest forms being more severe.