Harlequin Ichthyosis - Medical and Psychosocial Challenges

被引：5

作者：

Eilers, E. ^{[1
]}

Stieler, K. ^{[2
]}

Thies, C. ^{[3
]}

Blume-Peytavi, U. ^{[2
]}

Obladen, M. ^{[1
]}

Hueseman, D. ^{[1
]}

机构：

[1] Charite, Klin Neonatol, D-13353 Berlin, Germany

[2] Charite, Dermatol Klin, D-13353 Berlin, Germany

[3] Waldkrankenhaus Spandau, Kinderklin, Berlin, Germany

来源：

KLINISCHE PADIATRIE | 2010年 / 222卷 / 02期

关键词：

harlequin ichthyosis; compartment syndrome; ichthyosis congenita gravis; neonate; skin disease; ABCA12; MUTATIONS; THERAPY;

D O I：

10.1055/s-0029-1220943

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Harlequin ichthyosis is the most severe congenital keratinizing disorder. It is caused by mutations in the ABCA12 gene leading to defective lipid transport. The infants are born with ectropion, eclabium and fissured plate-like skin. Today these infants can survive with neonatal intensive care and retinoid therapy and need long-term interdisciplinary treatment in order to improve quality of life. How ever, the outcome in our case is impaired by severe psychomotor developmental delay, which has not yet been associated with Harlequin Ichthyosis.

引用

页码：86 / 89

页数：4

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