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GTR Home > Conditions/Phenotypes > Xeroderma pigmentosum group B

Xeroderma pigmentosum group B

Synonyms
ERCC3-Related Xeroderma Pigmentosum; XERODERMA PIGMENTOSUM B/COCKAYNE SYNDROME; XP, GROUP B; XPB/CS; Xeroderma pigmentosum, complementation group b

Summary

Excerpted from the GeneReview: Xeroderma Pigmentosum
Xeroderma pigmentosum (XP) is characterized by: Acute sun sensitivity (severe sunburn with blistering, persistent erythema on minimal sun exposure) with marked freckle-like pigmentation of the face before age two years; Sunlight-induced ocular involvement (photophobia, severe keratitis, atrophy of the skin of the lids, ocular surface neoplasms); Greatly increased risk of sunlight-induced cutaneous neoplasms (basal cell carcinoma, squamous cell carcinoma, melanoma) within the first decade of life. Approximately 25% of affected individuals have neurologic manifestations (acquired microcephaly, diminished or absent deep tendon stretch reflexes, progressive sensorineural hearing loss, progressive cognitive impairment, and ataxia). The most common causes of death are skin cancer, neurologic degeneration, and internal cancer. The median age at death in persons with XP with neurodegeneration (29 years) was found to be younger than that in persons with XP without neurodegeneration (37 years).
Full text of GeneReview (by section):
Summary
Diagnosis
Clinical Characteristics
Genetically Related (Allelic) Disorders
Differential Diagnosis
Management
Genetic Counseling
Resources
Molecular Genetics
Chapter Notes
References
Authors:
Kenneth H Kraemer
John J DiGiovanna
Deborah Tamura
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Available tests

36 tests are in the database for this condition.

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Clinical tests (36 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: BTF2, GTF2H, RAD25, Ssl2, TFIIH, TTD2, XPB, ERCC3
    Summary: ERCC excision repair 3, TFIIH core complex helicase subunit

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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