Trichothiodystrophy (Q87733): Difference between revisions
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13 August 2026
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Latest revision as of 13:38, 15 August 2026
Trichothiodystrophy is a heterogeneous group disorders characterised by short, brittle hair with low-sulphur content (due to an abnormal synthesis of the sulphur containing keratins). Within the spectrum of the TTD syndromes are numerous syndromes affecting mainly organs derived from the neuroectoderm. The clinical appearance is always characterised by brittle and fragile hair, often combined with growth retardation and intellectual deficit, congenital ichthyosis and nail abnormalities, among other symptoms.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1366758649 |
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| English | Trichothiodystrophy |
Trichothiodystrophy is a heterogeneous group disorders characterised by short, brittle hair with low-sulphur content (due to an abnormal synthesis of the sulphur containing keratins). Within the spectrum of the TTD syndromes are numerous syndromes affecting mainly organs derived from the neuroectoderm. The clinical appearance is always characterised by brittle and fragile hair, often combined with growth retardation and intellectual deficit, congenital ichthyosis and nail abnormalities, among other symptoms. |
Statements
CID11:ID_1366758649
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dki-india-ID_1366758649
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Concluído
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13 August 2026
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