Case report: Prolonged collodion membrane causing constrictive bands of the digits and treatment

Dermatology Online Journal

Volumn 16, Issue 1, 2010, Pages

  Roberts, Jennifer B ^a   Adelson, David ^a  

^a UNIVERSITY OF OKLAHOMA HEALTH SCIENCES CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE; PYROXYLIN; TRANSGLUTAMINASE 1;

ARTICLE; CASE REPORT; DESQUAMATION; EDEMA; ERYTHEMA; FEMALE; FINGER; FOLLOW UP; GENE MUTATION; HUMAN; INFANT; LAMELLAR ICHTHYOSIS; LIGATION; PAIN; GENETICS; HAND MALFORMATION; HETEROZYGOTE; ISCHEMIA; MISSENSE MUTATION; PATHOLOGY; POINT MUTATION; RNA SPLICING; VASCULARIZATION;

EDEMA; ERYTHEMA; FEMALE; FINGERS; HAND DEFORMITIES, CONGENITAL; HETEROZYGOTE; HUMANS; ICHTHYOSIS, LAMELLAR; INFANT; ISCHEMIA; MUTATION, MISSENSE; POINT MUTATION; RNA SPLICE SITES; TRANSGLUTAMINASES;

EID: 75749146233     PISSN: None     EISSN: 10872108     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Farasat J et al. Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA. J Med Genet. 2009;46:103-111.
2. Van Gysel, Lijnen RLP et al. Collodion baby: a follow-up study of 17 cases. Eur Acad Dermatol Venereol. 2002;16(5):472-5. [PubMed]
3. Oji V. Traupe H. Ichthyoses: Differential diagnosis and molecular genetics. Eur J Dermatol. 2006 Jul-Aug;16(4)349-59. [PubMed]
4. Schmuth M. Gruber R. Elias PM. Williams ML. Ichthyosis update: Towards a function-driven model of pathogenesis of the disorders of cornification and the role of corneocyte proteins in these disorders. Adv Dermatol. 2007;23:231-56. [PubMed]
5. Akiyama M. Sawamura D. Shimizu H. The clinical spectrum of nonbullous congenital ichthyosiform erythroderma and lamellar ichthyosis. Clin Exp Dermatol. 2003 May;28(3):235-40. [PubMed]
6. Shwayder T. Disorders of keratinization: diagnosis and management. Am J Clin Dermatol. 2004;5(1):17-29. Review. [PubMed]