共 10 条
Epidermal Nevus Syndrome Associated with Dwarfism and Atopic Dermatitis
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作者:

Mizutani, Yuki
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机构:
Gifu Prefectural Gen Med Ctr, Dept Dermatol, Gifu 5008717, Japan Gifu Prefectural Gen Med Ctr, Dept Dermatol, Gifu 5008717, Japan

Nagai, Miki
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机构:
Gifu Prefectural Gen Med Ctr, Dept Dermatol, Gifu 5008717, Japan Gifu Prefectural Gen Med Ctr, Dept Dermatol, Gifu 5008717, Japan

Iwata, Hitoshi
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机构:
Gifu Prefectural Gen Med Ctr, Dept Pathol, Gifu 5008717, Japan Gifu Prefectural Gen Med Ctr, Dept Dermatol, Gifu 5008717, Japan

Matsunami, Kunihiro
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机构:
Gifu Prefectural Gen Med Ctr, Dept Pediat, Gifu 5008717, Japan Gifu Prefectural Gen Med Ctr, Dept Dermatol, Gifu 5008717, Japan

Seishima, Mariko
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机构:
Gifu Univ, Dept Dermatol, Grad Sch Med, Gifu 5011194, Japan Gifu Prefectural Gen Med Ctr, Dept Dermatol, Gifu 5008717, Japan
机构:
[1] Gifu Prefectural Gen Med Ctr, Dept Dermatol, Gifu 5008717, Japan
[2] Gifu Prefectural Gen Med Ctr, Dept Pathol, Gifu 5008717, Japan
[3] Gifu Prefectural Gen Med Ctr, Dept Pediat, Gifu 5008717, Japan
[4] Gifu Univ, Dept Dermatol, Grad Sch Med, Gifu 5011194, Japan
来源:
CHILDREN-BASEL
|
2021年
/
8卷
/
08期
关键词:
epidermal nevus syndrome;
FGFR3;
Garcia-Hafner-Happle syndrome;
dwarfism;
atopic dermatitis;
FGFR3;
MUTATIONS;
D O I:
10.3390/children8080697
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
Epidermal nevus syndrome (ENS) is a congenital disorder characterized by widespread linear epidermal lesions consisting of epidermal nevus and extracutaneous involvements, especially of the central nervous system and skeletal system. Garcia-Hafner-Happle syndrome, also known as fibroblast growth factor receptor 3 (FGFR3)-ENS, is characterized by a systematized keratinocytic EN of soft and velvety type with neurological abnormalities such as seizures, intellectual impairment, and cortical atrophy. We present a case of a 9-year-old Japanese boy afflicted with Garcia-Hafner-Happle syndrome associated with dwarfism and atopic dermatitis. We show the results of physical examination, DNA analysis, and imaging studies and discuss the mutation underlying the child's disorder.
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