Lowe syndrome with extremely short stature: growth hormone deficiency may be the pathogeny-Reference-Cited by-同舟云学术

Lowe syndrome with extremely short stature: growth hormone deficiency may be the pathogeny

Published:2019-07-04 Issue:3-4 Volume:37 Page:170-177
ISSN:0897-7194
Container-title:Growth Factors
language:en
Short-container-title:Growth Factors

Author:

Dai Chengjun¹,Wang Liying²,Li Youli¹,Zheng Zhichao¹,Qian Jieqi¹,Wang Chaoban¹,Liu Zishuo¹,Shan Xiaoou¹

Affiliation:

1. Department of Pediatrics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou Medical University, Wenzhou, Zhejiang, PR China;

2. Beijing Tongren Hospital, Capital Medical University, Beijing, PR China

Publisher

Informa UK Limited

Subject

Cell Biology,Clinical Biochemistry,Endocrinology

Link

https://www.tandfonline.com/doi/pdf/10.1080/08977194.2019.1669589

Reference20 articles.

1. “Lowe syndrome: A particularly severe phenotype without clinical kidney involvement”

2. Phosphatidylinositol-4,5-bisphosphate: Actin Dynamics and the Regulation of ATP-Dependent and -Independent Secretion

3. Renal Phenotype in Lowe Syndrome: A Selective Proximal Tubular Dysfunction

4. The oculocerebrorenal syndrome of Lowe: an update

5. Clinical and Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Reference to Growth and Renal Function

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1. Short Stature due to Bioinactive Growth Hormone (Kowarski Syndrome);Endocrine Practice;2023-11

2. Novel pathogenic OCRL mutations and genotype–phenotype analysis of Chinese children affected by oculocerebrorenal syndrome: two cases and a literature review;BMC Medical Genomics;2021-09-06

3. Lowe Syndrome: A Complex Clinical Diagnosis with a Novel Mutation in the OCRL Gene;Journal of Child Science;2021-01