Literature DB >> 2097357

Congenital lipodystrophy with defective leucocyte function (a case report).

A S Kher1, K R Lahiri, M K Jain, M D Shah.   

Abstract

A 6 1/2 year old female child with congenital lipodystrophy is being presented. The noteworthy feature in this case was the defective leucocyte function and its association with tuberculous pericardial effusion.

Entities:  

Mesh：

Year:  1990        PMID： 2097357

Source DB:  PubMed          Journal:  J Postgrad Med        ISSN： 0022-3859            Impact factor:   1.476


  3 in total

1.  Congenital generalized lipodystrophy in an Indian patient with a novel mutation in BSCL2 gene.

Authors:  H U Shirwalkar; Z M Patel; J Magre; P Hilbert; L Van Maldergem; R R Mukhopadhyay; A Maitra
Journal:  J Inherit Metab Dis       Date:  2008-08-12       Impact factor: 4.982

2.  Berardinelli-Seip syndrome type 1 in an Egyptian child.

Authors:  Kotb Abbass Metwalley; Hekma Saad Farghaly
Journal:  Indian J Hum Genet       Date:  2014-01

3.  Berardinelli-Seip congenital lipodystrophy in two siblings.

Authors:  T S Mohana Rao; Kavya Chennamsetty
Journal:  Indian Dermatol Online J       Date:  2014-11
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.