Literature DB >> 17656942

Monilethrix.

G R Narmatha1, S Chithra, N Balasubramanian.   

Abstract

Monilethrix is rare hereditary disorder which is in herited as autosomal dominant trit. We report two siblings with a combination of monilethrix and leukonychia.

Entities:  

Year:  2002        PMID: 17656942

Source DB:  PubMed          Journal:  Indian J Dermatol Venereol Leprol        ISSN: 0378-6323            Impact factor:   2.545


  3 in total

1.  Monilethrix: a rare hereditary condition.

Authors:  Adaikalampillai Ganapathy Vikramkumar; Sheela Kuruvila; Satyaki Ganguly
Journal:  Indian J Dermatol       Date:  2013-05       Impact factor: 1.494

2.  Monilethrix in three generations.

Authors:  Gurcharan Singh; K Siddalingappa; K C Nischal; L Chandra Naik; K Lokanatha
Journal:  Indian J Dermatol       Date:  2008       Impact factor: 1.494

3.  Monilethrix: A Report of Three Cases in Children Confirmed with Dermoscopy.

Authors:  Remya R Rajamohanan; Biswanath Behera; Prabhakaran Nagendran; Munisamy Malathi
Journal:  Indian Dermatol Online J       Date:  2020-01-13
  3 in total

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