A Case of Nevoid Basal Cell Syndrome Associated with a Novel <i>PTCH1</i> Gene Mutation-Reference-Cited by-同舟云学术

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A Case of Nevoid Basal Cell Syndrome Associated with a Novel <i>PTCH1</i> Gene Mutation

Published:2023-12-01 Issue:6 Volume:85 Page:466-469
ISSN:0386-9784
Container-title:The Nishinihon Journal of Dermatology
language:en
Short-container-title:Nishinihon J Dermatol

Author:

NAKAGAWA Koichi¹,TOHDA Rie¹,TOKUDA Ichizo¹,MATSUO Ayako¹,OKABAYASHI Aya²,SHIMOMURA Yutaka³

Affiliation:

1. Department of Dermatology, Osaka-fu Saiseikai Tondabayashi Hospital

2. Department of Dermatology, Izumi City General Hospital

3. Department of Dermatology, Yamaguchi University Graduate School of Medicine

Publisher

Western Japan Division of JDA

Link

https://www.jstage.jst.go.jp/article/nishinihonhifu/85/6/85_466/_pdf

Reference15 articles.

1. 1) Kimonis VE, Goldstein AM, Pastakia B et al : Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome. Am J Med Genet, 1997 ; 69 : 299-308.

2. 2) 宮下俊之, 高山吉永 : Gorlin 症候群の遺伝子診断. 医のあゆみ, 2019 ; 268 : 123-126.

3. 3) Binkley GW, Johnson HH Jr. : Epithelioma adenoids cysticum : basal cell nevi, agenesis of the corpus callosum and dental cysts ; a clinical and autopsy study. AMA Arch Derm Syphilol, 1951 ; 63 : 73-84.

4. 4) 塩浜　直 : Gorlin 症候群の歴史. 医のあゆみ, 2019 ; 268 : 111-113.

5. 5) Gorlin RJ, Goltz RW : Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib. A syndrome. N Engl J Med, 1960 ; 262 : 908-912.

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