Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?-Reference-Cited by-同舟云学术

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Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?

Published:2004-07 Issue:4 Volume:21 Page:486-490
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatr Dermatol

Author:

Erbagci Zulal,Erbagci Ibrahim,Erbagci Hulya,Erkilic Suna,Tuncel A. Almila

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology and Child Health

Reference19 articles.

1. Monilethrix and Pseudo-Monilethrix

2. Monilethrix: a clinicopathological illustration of a cortical defect

3. Alopecia in a 19-month-old boy. Monilethrix

4. Hyperkeratotic Nodule

5. Medical Pearl: An easy way to diagnose severe neonatal monilethrix

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical and genetic aspects of a child with monilethrix and visual rehabilitation;Indian Journal of Ophthalmology - Case Reports;2022

2. Keratosis Pilaris and its Subtypes: Associations, New Molecular and Pharmacologic Etiologies, and Therapeutic Options;American Journal of Clinical Dermatology;2018-07-24

3. Literatur;Atlas der Pädiatrischen Dermatologie;2018-07-11

4. Genetic Hair Disorders;Pediatric Skin of Color;2015

5. Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix;Chinese Medical Journal;2013-08-30

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