Language delay and developmental catch-up would be a clinical feature of pseudohypoparathyroidism type 1A during childhood-Reference-Cited by-同舟云学术

Language delay and developmental catch-up would be a clinical feature of pseudohypoparathyroidism type 1A during childhood

Published:2019 Issue:3 Volume:66 Page:215-221
ISSN:0918-8959
Container-title:Endocrine Journal
language:en
Short-container-title:Endocr J

Author:

Miyakawa Yuichi¹,Takasawa Kei¹,Matsubara Yohei¹,Ihara Kenji²,Ohtsu Yoshiaki³,Kamasaki Hotaka⁴,Kitsuda Kazuteru⁵,Kobayashi Hironori⁶,Satoh Mari⁷,Sano Sinichiro⁸,Dateki Sumito⁹,Mochizuki Hiroshi¹⁰,Yokota Ichiro¹¹,Hasegawa Yukihiro¹²,Kashimada Kenichi¹

Affiliation:

1. Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo 113-8510, Japan

2. Department of Pediatrics, Oita University Faculty of Medicine, Oita 879-5593, Japan

3. Department of Pediatrics, Gunma University Graduate School of Medicine, Gunma 371-8511, Japan

4. Department of Pediatrics, Sapporo Medical University School of Medicine, Hokkaido 060-8543, Japan

5. Department of Pediatrics, Kitasato University, Kanagawa 252-0375, Japan

6. Department of Pediatrics, Shimane University Faculty of Medicine, Shimane 690-8501, Japan

7. Department of Pediatrics, Toho University Omori Medical Center, Tokyo 143-8541, Japan

8. Department of Pediatrics, Hamamatsu University School of Medicine, Shizuoka 431-3192, Japan

9. Department of Pediatrics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8501, Japan

10. Division of Endocrinology and Metabolism, Saitama Children’s Medical Center, Saitama 330-8777, Japan

11. Division of Pediatric Endocrinology and Metabolism, Shikoku Medical Center for Children and Adults, Kagawa 765-8507, Japan

12. Division of Endocrinology and Metabolism, Tokyo Metropolitan Children’s Medical Center, Tokyo 183-8561, Japan

Publisher

Japan Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.jstage.jst.go.jp/article/endocrj/66/3/66_EJ18-0326/_pdf

Reference16 articles.

1. 1 Long DN, McGuire S, Levine MA, Weinstein LS, Germain-Lee EL (2007) Body mass index differences in pseudohypoparathyroidism type 1a versus pseudopseudohypoparathyroidism may implicate paternal imprinting of Gαs in the development of human obesity. J Clin Endocrinol Metab 92: 1073–1079.

2. 2 De Sanctis L, Giachero F, Mantovani G, Weber G, Salerno M, et al. (2016) Genetic and epigenetic alterations in the GNAS locus and clinical consequences in Pseudohypoparathyroidism: Italian common healthcare pathways adoption. Ital J Pediatr 42: 101.

3. 3 Usardi A, Mamoune A, Nattes E, Carel JC, Rothenbuhler A, et al. (2017) Progressive development of PTH resistance in patients with inactivating mutations on the maternal allele of GNAS. J Clin Endocrinol Metab 102: 1844–1850.

4. 4 de Wijin EM, Steendijk R (1982) Growth and maturation in pseudohypoparathyroidism: a longitudinal study in 5 patients. Acta Endocrinol (Copenh) 101: 223–226.

5. 5 Mouallem M, Shaharabany M, Weintrob N, Shalitin S, Nagelberg N, et al. (2008) Cognitive impairment is prevalent in pseudohypoparathyroidism type Ia, but not in pseudopseudohypoparathyroidism: possible cerebral imprinting of Gsα. Clin Endocrinol (Oxf) 68: 233–239.

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