Article citationsMore>>
Brown, R.J., Araujo-Vilara, D., Cheung, T.P., Dunger, D., Garg, A., Jack, M., Mungai, L., Oral, E.A., Patni, N., Rother, K., von Schnurbein, J.J., Sorkina, E., Stanley, T., Vigouroux, C., Wabitsch, M., Williams, R. and Yorifuji, T. (2016) The Diagnosis and Management of Lipodystrophy Syndromes: A Multi-Society Practice Guideline. The Journal of Clinical Endocrinology & Metabolism, 101, 4500-4511.
https://doi.org/10.1210/jc.2016-2466
has been cited by the following article:
-
TITLE:
Congenital Lipodystrophy: A Case Series Report from Cameroon
AUTHORS:
Suzanne Sap Ngo Um, Jocelyn Tony, Ritha Mbono, Yannick Tekel, Isabelle Mekone, Mesmin Dehayem, Koki Ndombo
KEYWORDS:
Lipodystrophy, Diabetes, Children
JOURNAL NAME:
Open Journal of Pediatrics,
Vol.10 No.1,
March
26,
2020
ABSTRACT: Congenital lipodystrophy is a group of rare syndrome characterized by the absence of subcutaneous tissue. Affecting less per million live birth, this condition associate metabolic disturbance including severe insulin resistance and progeroid appearance. Diagnosis may be fortuitous or related to complications as presented in the present case series. Lipodystrophy can be generalized or localized. Acquired lipodystrophy is associated with some drugs like antiretroviral. Thus, the condition is well described in African HIV patients but data on congenital forms from Sub Saharan Africa are sparse, justifying the present report. We present four cases, with peculiar appearance associated with increased blood triglycerides. Two on four of the patients presented diabetes mellitus. Genetic testing was not available, questioning the actual guidelines of diagnosis for our context.
Related Articles:
-
Guijun Xie, Songwen Zhang
-
R. Douglas Martin, Shengyu Zhang
-
Tiama Guy Nicaise Ballet, Kôkôh Rose Effebi, Olga Yolande Aké Ako, Yapo Habib Kpidi, Ossey Bernard Yapo
-
Hervé A. N’cho, Innocent K. Kouame, Kouadio Koff, Lazare K. Kouassı, Séraphin K. Konan, Ruth Baï, Andrei Sandu, Ion Sandu
-
Espen Gaarder Haug