Keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK syndrome);Queratosis linear con ictiosis congénita y queratodermia esclerosante (síndrome KLICK)

Actas Dermo-Sifiliograficas

Volumn 97, Issue 5, 2006, Pages 342-344

  Chaves, Antonio J ^a   Merchan Garcia R ^a   Fernández Recio, José Ma ^a   Rodríguez Nevado, Isabel ^a   De Argila, Diego ^a  

^a HOSPITAL INFANTA CRISTINA   (Spain)

Author keywords

Ichthyosis; Keratoderma

Indexed keywords

EMOLLIENT AGENT; RETINOID; UREA;

ADULT; ARTICLE; CASE REPORT; CLINICAL EXAMINATION; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; EPIDERMIS HYPERPLASIA; HUMAN; HYPERKERATOSIS; KERATODERMA; KERATOSIS; KERATOSIS PALMOPLANTARIS; KLICK SYNDROME; MALE; SKIN DISEASE; SKINFOLD;

EID: 33746383979     PISSN: 00017310     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0001-7310(06)73415-9     Document Type: Article

References (7)

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2. Vahlquist A, Ponten F, Pettersson A. Keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK-syndrome): A rare, autosomal recessive disorder of keratohyaline formation? Acta Derm Venereol. 1997;77:225-7.
3. Vahlquist A, Ganemo A, Pigg M, Virtanen M, Westermark P. The clinical spectrum of congenital ichthyosis in Sweden: a review of 127 cases. Acta Derm Venereol. 2003;213 Suppl: 34-47.
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6. Maestrini E, Mónaco AP, McGrath JA, et al. A molecular defect in loricrin, the mayor component of the cornified cell envelope, underlies Vohwinke's syndrome. Nature Genet. 1996;13:70-7.
7. Sprecher E, Ishida-Yamamoto A, Mizrahi-Koren M, et al. A mutation in SNAP29, coding for a SNARE protein involved in intracelullar trafficking, causes a novel neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratodermia. Am J Hum Genet. 2005;77:242-51.