You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 144 No. 3, March 2008 TABLE OF CONTENTS
  Archives
  •  Online Features
  Observation
 This Article
 •Full text
 •PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Contact me when this article is cited
 Related Content
 •Related articles
 •Similar articles in this journal
 Topic Collections
 •Genetics
 •Pediatrics
 •Congenital Malformations
 •Neonatology and Infant Care
 •Dermatologic Disorders, Other
 •Alert me on articles by topic

Self-Healing Collodion Membrane and Mild Nonbullous Congenital Ichthyosiform Erythroderma Due to 2 Novel Mutations in the ALOX12B Gene

Mandy Harting, MD; Nicola Brunetti-Pierri, MD; C. Stanley Chan, MD; Joslyn Kirby, MD; Megan K. Dishop, MD; Gabriele Richard, MD; Fernando Scaglia, MD; Albert C. Yan, MD; Moise L. Levy, MD

Arch Dermatol. 2008;144(3):351-356.

Background  Collodion phenotype is a term applied to the condition affecting a newborn involving a parchmentlike membrane covering the whole body surface (collodion membrane). This presentation is common to several different forms of autosomal recessive congenital ichthyoses, including nonbullous congenital ichthyosiform erythroderma (NCIE), lamellar ichthyosis (LI), and harlequin ichthyosis (HI). Recent years have seen considerable advances in our understanding of the molecular basis of autosomal recessive forms of congenital ichthyosis. Several genetic loci have been identified for LI and NCIE.

Observations  We describe the clinical and molecular features of 2 cases of self-healing newborns of collodion phenotype developing mild NCIE. A dramatic improvement of the skin was observed in the first few weeks after birth in both cases. The molecular analysis of the ALOX12B gene demonstrated that both patients were compound heterozygous for previously unreported mutations.

Conclusions  Both patients were compound heterozygous for novel ALOX12B mutations, underscoring the concept that mutations in at least 2 different genes, ALOX12B and TGM1, may result in this unusual clinical phenotype.


Author Affiliations: Departments of Dermatology (Drs Harting, Chan, and Levy), Genetics (Drs Brunetti-Pierri and Scaglia), Pathology (Dr Dishop), and Pediatrics (Dr Levy), Texas Children's Hospital, Baylor College of Medicine, Houston; Department of Molecular and Human Genetics, Baylor College of Medicine (Drs Brunetti-Pierri and Scaglia); The Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia (Drs Kirby and Yan); and GeneDx Inc, Gaithersburg, Maryland (Dr Richard). Dr Levy is now with ’Specially for Children, Austin, Texas.


RELATED ARTICLES

Molecular Genetics as a Diagnostic and Prognostic Aid in the Assessment of Neonates With Red, Scaly Genodermatoses: Work Still in Progress
Suzanne E. Clements and John A. McGrath
Arch Dermatol. 2008;144(3):387-388.
EXTRACT | FULL TEXT  

Dermatology in the Postgenomic Era: Harnessing Human Variation for Personalized Medicine
Anthony E. Oro
Arch Dermatol. 2008;144(3):389-391.
EXTRACT | FULL TEXT  


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Molecular Genetics as a Diagnostic and Prognostic Aid in the Assessment of Neonates With Red, Scaly Genodermatoses: Work Still in Progress
Clements and McGrath
Arch Dermatol 2008;144:387-388.
FULL TEXT  

Dermatology in the Postgenomic Era: Harnessing Human Variation for Personalized Medicine
Oro
Arch Dermatol 2008;144:389-391.
FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2008 American Medical Association. All Rights Reserved.