Congenital generalized lipodystrophy in children: Berardinelli–Seip syndrome – two rare cases with renal manifestations

Berardinelli–Seip syndrome is a rare autosomal recessive disorder characterized by an almost total lack of subcutaneous fat with various metabolic abnormalities and complications such as diabetes mellitus and insulin resistance. Renal changes and complications are uncommon but reported. We present t...

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Main Authors: S Satya, Gandikota Raghu Rama Rao, K Prathima, D Lavanya, K Sandeep, A Amareswar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Indian Journal of Paediatric Dermatology
Subjects:
Online Access:http://www.ijpd.in/article.asp?issn=2319-7250;year=2017;volume=18;issue=3;spage=227;epage=229;aulast=Satya
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spelling doaj-6f545396f10e4841abf9ecbb366bedf92020-11-25T00:02:17ZengWolters Kluwer Medknow PublicationsIndian Journal of Paediatric Dermatology2319-72502017-01-0118322722910.4103/2319-7250.193008Congenital generalized lipodystrophy in children: Berardinelli–Seip syndrome – two rare cases with renal manifestationsS SatyaGandikota Raghu Rama RaoK PrathimaD LavanyaK SandeepA AmareswarBerardinelli–Seip syndrome is a rare autosomal recessive disorder characterized by an almost total lack of subcutaneous fat with various metabolic abnormalities and complications such as diabetes mellitus and insulin resistance. Renal changes and complications are uncommon but reported. We present two such rare cases with renal involvement.http://www.ijpd.in/article.asp?issn=2319-7250;year=2017;volume=18;issue=3;spage=227;epage=229;aulast=SatyaAcanthosis nigricansBerardinelli–Seip syndromecongenital generalized lipodystrophyhypertrichosisrenal changes
collection DOAJ
language English
format Article
sources DOAJ
author S Satya
Gandikota Raghu Rama Rao
K Prathima
D Lavanya
K Sandeep
A Amareswar
spellingShingle S Satya
Gandikota Raghu Rama Rao
K Prathima
D Lavanya
K Sandeep
A Amareswar
Congenital generalized lipodystrophy in children: Berardinelli–Seip syndrome – two rare cases with renal manifestations
Indian Journal of Paediatric Dermatology
Acanthosis nigricans
Berardinelli–Seip syndrome
congenital generalized lipodystrophy
hypertrichosis
renal changes
author_facet S Satya
Gandikota Raghu Rama Rao
K Prathima
D Lavanya
K Sandeep
A Amareswar
author_sort S Satya
title Congenital generalized lipodystrophy in children: Berardinelli–Seip syndrome – two rare cases with renal manifestations
title_short Congenital generalized lipodystrophy in children: Berardinelli–Seip syndrome – two rare cases with renal manifestations
title_full Congenital generalized lipodystrophy in children: Berardinelli–Seip syndrome – two rare cases with renal manifestations
title_fullStr Congenital generalized lipodystrophy in children: Berardinelli–Seip syndrome – two rare cases with renal manifestations
title_full_unstemmed Congenital generalized lipodystrophy in children: Berardinelli–Seip syndrome – two rare cases with renal manifestations
title_sort congenital generalized lipodystrophy in children: berardinelli–seip syndrome – two rare cases with renal manifestations
publisher Wolters Kluwer Medknow Publications
series Indian Journal of Paediatric Dermatology
issn 2319-7250
publishDate 2017-01-01
description Berardinelli–Seip syndrome is a rare autosomal recessive disorder characterized by an almost total lack of subcutaneous fat with various metabolic abnormalities and complications such as diabetes mellitus and insulin resistance. Renal changes and complications are uncommon but reported. We present two such rare cases with renal involvement.
topic Acanthosis nigricans
Berardinelli–Seip syndrome
congenital generalized lipodystrophy
hypertrichosis
renal changes
url http://www.ijpd.in/article.asp?issn=2319-7250;year=2017;volume=18;issue=3;spage=227;epage=229;aulast=Satya
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