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DeCS
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Descriptor English:
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Trichothiodystrophy Syndromes
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Descriptor Spanish:
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Síndromes de Tricotiodistrofia
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Descriptor Portuguese:
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Síndromes de Tricotiodistrofia
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Synonyms English:
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Amish Brittle Hair Brain Syndrome
Amish Brittle Hair Syndrome
BIDS Syndrome
BIDS Syndromes
Brittle Hair Intellectual Impairment Decreased Fertility Short Stature Syndrome
Brittle Hair-Intellectual Impairment-Decreased Fertility-Short Stature Syndrome
Hair Brain Syndrome
Hair-Brain Syndrome
Hair-Brain Syndromes
IBIDS Syndrome
IBIDS Syndromes
Ichthyosiform Erythroderma with Hair Abnormality and Mental and Growth Retardation
Ichthyosis, Brittle Hair, Intellectual Impairment, Decreased Fertility, and Short Stature
PIBIDS Syndrome
PIBIDS Syndromes
Photosensitive Trichothiodystrophies
Photosensitive Trichothiodystrophy
Tay Syndrome
Trichothiodystrophies
Trichothiodystrophies, Nonphotosensitive 1
Trichothiodystrophies, Photosensitive
Trichothiodystrophy
Trichothiodystrophy Syndrome
Trichothiodystrophy with Congenital Ichtyosis
Trichothiodystrophy, Nonphotosensitive 1
Trichothiodystrophy, Photosensitive
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Tree Number:
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C16.131.077.899
C16.131.831.874
C16.320.850.895
C17.800.804.874
C17.800.827.895
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Definition English:
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Autosomal recessive neuroectodermal disorders characterized by brittle sulfur-deficient hair associated with impaired intellect, decreased fertility, and short stature. It may include nail dystrophy, ICHTHYOSIS, and photosensitivity correlated with a NUCLEOTIDE EXCISION REPAIR defect. All individuals with this disorder have a deficiency of cysteine-rich KERATIN-ASSOCIATED PROTEINS found in the interfilamentous matrix. Photosensitive trichothiodystrophy can be caused by mutation in at least 2 separate genes: ERCC2 PROTEIN gene and the related ERCC3. Nonphotosensitive trichothiodystrophy can be caused by mutation in the TTDN1 gene. |
See Related English:
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Xeroderma Pigmentosum Group D Protein
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History Note English:
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2008
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Allowable Qualifiers English:
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Record Number:
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52625
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Unique Identifier:
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D054463
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Occurrence in VHL:
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Similar:
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DeCS
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