Genetic syndrome with ichthyosis: Congenital ichthyosis, follicular atrophoderma, hypotrichosis, and woolly hair; second report [1]

British Journal of Dermatology

Volumn 147, Issue 3, 2002, Pages 604-606

  Tursen, U ^a   Kaya, T I ^a   Ikizoglu, G ^a   Aktekin, M ^a   Aras, N ^a  

^a MERSIN UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ATROPHIC SKIN DISEASE; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; FEMALE; FOLLICULAR ATROPHODERMA; GENETIC DISORDER; HAIR ANALYSIS; HAIR DISEASE; HUMAN; HYPOTRICHOSIS; ICHTHYOSIS VULGARIS; KERATOSIS; LETTER; PRIORITY JOURNAL;

ADOLESCENT; ATROPHY; FEMALE; HAIR; HAIR FOLLICLE; HUMANS; HYPOTRICHOSIS; ICHTHYOSIS; SKIN DISEASES, GENETIC; SYNDROME;

EID: 0036042557     PISSN: 00070963     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2133.2002.48461.x     Document Type: Letter

References (10)

1. Disorders of keratinization
2. Congenital ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis: A new genodermatosis?
3. A Scottish family with Bazex-Dupre-Christol syndrome: Follicular atrophoderma, congenital hypotrichosis, and basal cell carcinoma
4. The Bazex-Dupre-Christol syndrome
5. Cholesterol metabolism defect associated with Conradi-Hunerman-Happle syndrome
6. Ichthyosiform dermatoses
7. Wooly hair: Clinical and general aspects
8. Wooly hair, palmoplantar keratoderma and cardiac abnormalities: Report of a family
9. Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)
10. Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma