Literature DB >> 27512436

A woman with familial partial lipodystrophy and the complications of her four pregnancies.

Simrit Nijjar1, Ken Laji2, Sophia Stone3.   

Abstract

We discuss a case of a woman ultimately diagnosed with familial partial lipodystrophy following her fourth pregnancy. In her previous pregnancies she had numerous complications thought to be related to diabetes including recurrent macrosomia and polyhydramnios. In her second pregnancy she underwent emergency caesarean section for fetal tachycardia at 34 weeks' gestation. Her baby was diagnosed with unexplained cerebral ischaemic injury and limb ischaemia requiring amputation. Postnatally she was diagnosed with type 2 diabetes mellitus with subsequent poor control. Very high insulin demands in this fourth pregnancy and an unusual phenotypic appearance in the patient and her mother raised suspicion of an underlying condition. Genetic studies confirmed the clinical diagnosis of familial partial lipodystrophy.

Entities:  

Keywords:  Clinical genetics; diabetes; high-risk pregnancy; maternal-fetal medicine; reproductive endocrinology

Year:  2014        PMID: 27512436      PMCID: PMC4934973          DOI: 10.1177/1753495X13516441

Source DB:  PubMed          Journal:  Obstet Med        ISSN: 1753-495X


  3 in total

1.  Fertility and obstetrical complications in women with LMNA-related familial partial lipodystrophy.

Authors:  M C Vantyghem; D Vincent-Desplanques; F Defrance-Faivre; J Capeau; C Fermon; A S Valat; O Lascols; A C Hecart; P Pigny; B Delemer; C Vigouroux; J L Wemeau
Journal:  J Clin Endocrinol Metab       Date:  2008-03-25       Impact factor: 5.958

2.  Adipose tissue distribution pattern in patients with familial partial lipodystrophy (Dunnigan variety).

Authors:  A Garg; R M Peshock; J L Fleckenstein
Journal:  J Clin Endocrinol Metab       Date:  1999-01       Impact factor: 5.958

3.  Overlapping syndrome with familial partial lipodystrophy, Dunnigan variety and cardiomyopathy due to amino-terminal heterozygous missense lamin A/C mutations.

Authors:  L Subramanyam; V Simha; A Garg
Journal:  Clin Genet       Date:  2009-12-22       Impact factor: 4.438

  3 in total

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