Ichthyosis prematurity syndrome caused by a novel fatty acid transport protein 4 gene mutation in a German infant

Arch Dermatol. 2011 Jun;147(6):750-2. doi: 10.1001/archdermatol.2011.139.

Authors

Oliver Inhoff, Ingrid Hausser, Stefan W Schneider, Denis Khnykin, Frode L Jahnsen, Johann Sartoris, Sergij Goerdt, Wiebke K Peitsch

PMID: 21690550
DOI: 10.1001/archdermatol.2011.139

No abstract available

Publication types

Case Reports
Letter
Research Support, Non-U.S. Gov't

MeSH terms

Aniridia
Anti-Infective Agents, Local / therapeutic use
Fatty Acid Transport Proteins / genetics*
Humans
Ichthyosis / drug therapy
Ichthyosis / genetics
Ichthyosis / pathology
Infant, Newborn
Infant, Premature, Diseases / drug therapy
Infant, Premature, Diseases / genetics
Infant, Premature, Diseases / pathology
Kidney / abnormalities
Male
Mutation*
Psychomotor Disorders
Treatment Outcome
Triclosan / therapeutic use

Substances

Anti-Infective Agents, Local
Fatty Acid Transport Proteins
SLC27A4 protein, human
Triclosan

Supplementary concepts

Ichthyosis prematurity syndrome