Cargando…
A Patient with Berardinelli-Seip Syndrome, Novel AGPAT2 Splicesite Mutation and Concomitant Development of Non-diabetic Polyneuropathy
Primary polyneuropathy in the context of Seip-Berardinelli type 1 seipinopathy, or congenital generalized lipodystrophy type 1 (CGL1) has not been previously reported. We report the case history of a 27 year old female CGL1 patient presenting with an unusual additional development of non-diabetic pe...
Autores principales: | Oswiecimska, Joanna, Dawidziuk, Mateusz, Gambin, Tomasz, Ziora, Katarzyna, Marek, Marta, Rzonca, Sylwia, Guilbride, D. Lys, Jhangiani, Shalini N., Obuchowicz, Anna, Sikora, Alicja, Lupski, James R., Wiszniewski, Wojciech, Gawlinski, Pawel |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745459/ https://www.ncbi.nlm.nih.gov/pubmed/30563316 http://dx.doi.org/10.4274/jcrpe.galenos.2018.2018.0227 |
Ejemplares similares
-
Berardinelli-Seip congenital lipodystrophy in two siblings
por: Rao, T. S. Mohana, et al.
Publicado: (2014) -
Berardinelli-Seip syndrome type 1 in an Egyptian child
por: Metwalley, Kotb Abbass, et al.
Publicado: (2014) -
Berardinelli-Seip syndrome and achalasia: a shared pathomechanism?
por: van der Pol, Rachel J., et al.
Publicado: (2015) -
Nurses' knowledge about Berardinelli-Seip Congenital Lipodystrophy
por: Cândido Dantas, Verônica Kristina, et al.
Publicado: (2018) -
Berardinelli-Seip Syndrome and Essential Thrombocytosis: An Unusual Association
por: Alzu’bi, Ali A., et al.
Publicado: (2020)