Disease name

IBIDS 증후군
 IBIDS syndrome

Marker gene

Gene symbol Chromosome location Protein name
ERCC2 19q13.32 TFIIH basal transcription factor complex helicase XPD subunit
ERCC3 2q14.3 TFIIH basal transcription factor complex helicase XPB subunit
GTF2H5 6q25.3 General transcription factor IIH subunit 5
TTDN1 7p14 TTD non-photosensitive 1 protein

Prevalence

<1 / 1 000 000

Inheritance

상염색체 열성

Age of onset

신생아기, 영아기

ICD 10 code

E72.1, Q80.8

MIM number

601675

Synonym

Tay syndrome
Trichothiodystrophy type E
Trichothiodystrophy with congenital ichthyosis

Summary

IBIDS syndrome (or Tay syndrome) is a form of trichothiodystrophy (sulfur-deficient brittle hair) characterized by Ichtyosis, Brittle hair, Intellectual impairment, Decreased fertility, and Short stature. Up to 1991, clinical data on 15 cases with IBIDS had been published. It is an autosomal recessive disorder, caused by a deficiency in sulfur-rich proteins. Diagnosis is based on the clinical signs, hair examination under polarized light, and biochemical evidence of the sulfur-containing amino acid deficiency (in particular cystine) in the hair. Antenatal diagnosis is feasible. There is no specific treatment.