Seipin-linked congenital generalized lipodystrophy type 2: a rare case with multiple lytic and pseudo-osteopoikilosis lesions

Congenital generalized lipodystrophy (CGL), or Berardinelli–Seip syndrome (BSCL), is a part of lipodystrophic syndromes that constitute a heterogeneous group of genetic or acquired generalized or partial body fat loss disorders. It is a rare autosomal recessive disease characterized by a near-absenc...

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Detalles Bibliográficos
Autores principales: Yamamoto, Asako, Kusakabe, Toru, Sato, Kenji, Tokizaki, Toru, Sakurai, Keita, Abe, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906354/
https://www.ncbi.nlm.nih.gov/pubmed/31853371
http://dx.doi.org/10.1177/2058460119892407

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906354/
https://www.ncbi.nlm.nih.gov/pubmed/31853371
http://dx.doi.org/10.1177/2058460119892407

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