Suppr超能文献

先天性厚甲症的口腔表现。病例报告。

Oral manifestations of pachyonychia congenita. Report of a case.

作者信息

Maser E D

出版信息

Oral Surg Oral Med Oral Pathol. 1977 Mar;43(3):373-8. doi: 10.1016/0030-4220(77)90323-1.

Abstract

Few cases of pachyonychia congenita are reported in the dental and medical literature because of the rarity of the disease. This article presents a review of the literature and adds a new case history. Examination of a 4-year-old boy revealed the presence of the disease, which was also present in the mother and a newborn sibling.

摘要

由于先天性厚甲症罕见,牙科和医学文献中报道的病例很少。本文对文献进行了综述,并增加了一个新的病例史。对一名4岁男孩的检查发现了该疾病,其母亲和新生儿同胞也患有该疾病。

相似文献

1
Oral manifestations of pachyonychia congenita. Report of a case.
Oral Surg Oral Med Oral Pathol. 1977 Mar;43(3):373-8. doi: 10.1016/0030-4220(77)90323-1.
3
[Jadassohn-Lewandowsky syndrome (pachyonychia congenita)].
Actas Dermosifiliogr. 1978 Jan-Feb;69(1-2):19-26.
4
Pachyonychia congenita (Jadassohn-Lewandowski syndrome: case report.
Plast Reconstr Surg. 1977 Jun;59(6):855-8. doi: 10.1097/00006534-197706000-00026.
5
[Type I pachyonychia congenita (Jadarssohn-Lewandowsky)].
Klin Padiatr. 1999 May-Jun;211(3):179-83. doi: 10.1055/s-2008-1043783.
6
Images in neonatal Medicine. Pachyonychia congenita.
Arch Dis Child Fetal Neonatal Ed. 2004 Sep;89(5):F467. doi: 10.1136/adc.2003.040485.
7
A case of pachyonychia congenita with oral leukoplakia and steatocystoma multiplex.
J Dermatol. 1999 Oct;26(10):677-81. doi: 10.1111/j.1346-8138.1999.tb02071.x.
8
Avoiding Pachyonychia congenita using oocyte donation.
Dermatology. 1999;198(1):107-8. doi: 10.1159/000018083.
9
Pachyonychia congenita. Case report.
Minerva Stomatol. 2005 Nov-Dec;54(11-12):691-4.
10
Dyskeratosis congenita with esophageal stricture and dermatological manifestations.
Endoscopy. 1994 Oct;26(8):711-2. doi: 10.1055/s-2007-1009076.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验