Lymphedema complicated by protein-losing enteropathy with a 22q13.3 deletion and the potential role of CELSR1: A case report

INTRODUCTION: 22q13.3 deletion syndrome is a well-known syndrome characterized by typical clinical findings including neonatal hypotonia, absent or severely delayed speech, intellectual disability, and other various features, and detection of a heterozygous deletion of chromosome 22q13.3 with the in...

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Detalles Bibliográficos
Autores principales: Xia, Song, Liu, Zhong, Yan, Huifang, Chang, Kun, Sun, Yuguang, Wang, Jingmin, Shen, Wenbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213278/
https://www.ncbi.nlm.nih.gov/pubmed/34128868
http://dx.doi.org/10.1097/MD.0000000000026307

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213278/
https://www.ncbi.nlm.nih.gov/pubmed/34128868
http://dx.doi.org/10.1097/MD.0000000000026307

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