Lamellar ichthyosis: A case report

Turkish Journal of Pediatrics

Volumn 44, Issue 1, 2002, Pages 58-60

  Özyürek, Hamit ^a   Kavak, Ayşe ^a   Alper, Murat ^a  

^a ABANT IZZET BAYSAL UNIVERSITY   (Turkey)

Author keywords

Ectropion; Lamellar ichthyosis; Treatment

Indexed keywords

2 HYDROXYACID; RETINOID; UREA;

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CHILD; CONSANGUINEOUS MARRIAGE; CONTROLLED STUDY; ECTROPION; HAIR DISEASE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERKERATOSIS; LAMELLAR ICHTHYOSIS; MALE; MEDICAL LITERATURE; NEUROLOGIC DISEASE; SIDE EFFECT; SKIN BIOPSY; SKIN DEFECT; SKIN EXFOLIATION;

CHILD, PRESCHOOL; HUMANS; ICHTHYOSIS, LAMELLAR; MALE;

EID: 0036170934     PISSN: 00414301     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

1. Autosomal-dominant lamellar ichthyosis: Ultrastructural characteristics of a new type of congenital ichthyosis
2. Unilateral magalocornea in lamellar ichthyosis
3. Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneity
4. Identification of mutations in the transglutaminase 1 gene in lamellar ichthyosis
5. Genetic and immunohistochemical detection of mutations inactivating the keratinocyte transglutaminase in patients with lamellar ichthyosis
6. Lamellar ichthyosis is genetically heterogenous-cases with normal keratinocyte transglutaminase
7. Topical treatment of ichthyoses and Darier's disease with 13-cis-retinoic acid. A clinical and immunohistochemical study
8. Ichthyosis in a nutshell