Literature DB >> 21779653

[Dunnigan-type familial partial lipodystrophy: attention to precocious diagnosis].

Lenora Maria Camarate Silveira Martins Leão1, Renata Carvalho de Alencar, Gisele da Cunha Rodrigues, Izabel Bouzas, Paulo Gallo, Ana Rossini.   

Abstract

Dunnigan-type familial partial lipodystrophy (FPLD) is an autosomal dominant disease that results from heterozygous missense mutations in LMNA, the gene that encodes nuclear lamin A/C. FPLD is characterized by a progressive disappearance of subcutaneous adipose tissue in the limbs, gluteal region, abdomen and trunk, beginning at the time of or after puberty, and excessive amount of fat in the face, chin, labia majora, and intra-abdominal region, leading to a Cushingoid appearance and increased muscularity phenotype. Affected women are particularly predisposed to insulin resistance and its complications, including features of polycystic ovary syndrome. To emphasize the importance of an early FPLD diagnosis, which is necessary to prevent serious metabolic disturbances, we report a woman diagnosed at about 50 years of age. Increased muscularity and significant labia majora fat deposit made the diagnosis possible by gynecologists.

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Year:  2011        PMID: 21779653     DOI: 10.1590/s0100-72032011000200008

Source DB:  PubMed          Journal:  Rev Bras Ginecol Obstet        ISSN: 0100-7203


  1 in total

Review 1.  Cardiac Alterations in Patients with Familial Lipodystrophy.

Authors:  Minna Moreira Dias Romano; Paula Ananda Inês Chacon; Fernanda Naira Zambelli Ramalho; Maria Cristina Foss; André Schmidt
Journal:  Arq Bras Cardiol       Date:  2020-02       Impact factor: 2.000

  1 in total

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