Pseudohypoparathyroidism type 1B – a rare cause of tetany: case report-Reference-Cited by-同舟云学术

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Pseudohypoparathyroidism type 1B – a rare cause of tetany: case report

Published:2017-06-26 Issue:4 Volume:38 Page:281-284
ISSN:2046-9047
Container-title:Paediatrics and International Child Health
language:en
Short-container-title:Paediatrics and International Child Health

Author:

Garcia Catarina¹,Correia Cátia R.²,Lopes Lurdes³

Affiliation:

1. Department of Pediatrics, Hospital Professor Doutor Fernando Fonseca, EPE, Lisbon, Portugal

2. Department of Pediatrics, Centro Hospitalar Lisboa Ocidental, EPE, Lisbon, Portugal

3. Endocrinology Unit, Department of Pediatrics, Centro Hospitalar Lisboa Central, EPE, Lisbon, Portugal

Publisher

Informa UK Limited

Subject

Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/20469047.2017.1341730

Reference24 articles.

1. Pseudohypoparathyroidism Type Ib Associated with Novel Duplications in the GNAS Locus

2. Neuromuscular symptoms in a patient with familial pseudohypoparathyroidism type Ib diagnosed by methylation-specific multiplex ligation-dependent probe amplification

3. Pseudohypoparathyroidism type Ib in 2015

4. Pseudohypoparathyroidism type I-b with neurological involvement is associated with a homozygousPTH1Rmutation

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1. Pseudohypoparathyroidism leading to bilateral hip fracture: A case report;Radiology Case Reports;2024-11

2. Pseudohypoparathyroidism type 1B with involuntary movements: a case report and literature review;CLIN PEDIATR ENDOCRI;2024

3. Pseudohypoparathyroidism type 1B with involuntary movements: a case report and literature review;Clinical Pediatric Endocrinology;2024

4. Pseudohypoparathyroidism type 1 B mimicking Fahr’s disease in a 28‐year‐old female: A case report;Clinical Case Reports;2022-02

5. Autosomal dominant pseudohypoparathyroidism type 1B due to STX16 deletion: a case presentation and literature review;Minerva Endocrinology;2022-02

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