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IBIDS syndrome

Orpha number ORPHA453
Prevalence of rare diseases <1 / 1 000 000
Inheritance
  • Autosomal recessive
Age of onset Neonatal/infancy
ICD 10 code
  • E72.1
  • Q80.8
MIM number
Synonym(s) 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. *Authors: Dr A. Rossi and Dr Cantisani (May 2006)*.

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
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