Suppr超能文献

1a型假性甲状旁腺功能减退伴关节屈曲畸形的一种新型GNAS突变:病例报告

A novel GNAS mutation in pseudohypoparathyroidism type 1a with articular flexion deformity: A case report.

作者信息

Wan Jinxing, He Dongjuan, Xie Jun, Chen Zhizhi

机构信息

Department of Endocrinology, The Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, 324000, Zhejiang, China.

Department of Orthopedics, The Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, No. 100 of Minjiang Avenue, Quzhou, 324000, Zhejiang, China.

出版信息

Open Life Sci. 2024 Jul 24;19(1):20220918. doi: 10.1515/biol-2022-0918. eCollection 2024.

Abstract

Pseudohypoparathyroidism (PHP) type 1a (PHP 1a) is a rare hereditary disorder characterized by target organ resistance to hormonal signaling and the Albright hereditary osteodystrophy (AHO) phenotype, which features round facial features, short fingers, subcutaneous calcifications, short stature, obesity, and intellectual disability. Progressive osseous heteroplasia (POH) is another rare disorder characterized by heterotopic ossification (HO) that progressively affects skin, subcutaneous tissues, and deep skeletal muscle. PHP 1a is inherited maternally due to a GNAS mutation, while pure POH is inherited paternally. This case study presented a Chinese boy with congenital hypothyroidism, tonic-clonic seizures, hypoparathyroidism, AHO, POH, and joint fixation deformity. Sequencing analysis of GNAS-Gsα revealed a heterozygous C.432+2T>C(P.?) variant (NM_000516.7) affecting the canonical splice donor site of intron 5 in the boy and his mother, indicating maternal inheritance of a GNAS mutation. The patient was diagnosed with POH overlap syndrome (POH/PHP 1a). Following calcium and calcitriol supplementation, he experienced a reduction in seizures, and surgery was performed to correct the joint fixation deformity caused by HO. This case report provided valuable insights into the genotype-phenotype correlations of POH overlap syndrome and underscored the significance of genetic testing in diagnosing rare diseases.

摘要

1a型假性甲状旁腺功能减退症(PHP 1a)是一种罕见的遗传性疾病,其特征为靶器官对激素信号传导的抵抗以及奥尔布赖特遗传性骨营养不良(AHO)表型,该表型具有圆脸、短指、皮下钙化、身材矮小、肥胖和智力残疾等特征。进行性骨化性纤维发育不良(POH)是另一种罕见的疾病,其特征为异位骨化(HO),逐渐影响皮肤、皮下组织和深部骨骼肌。PHP 1a由于GNAS突变而呈母系遗传,而纯POH呈父系遗传。本病例研究报告了一名患有先天性甲状腺功能减退症、强直阵挛性癫痫、甲状旁腺功能减退症、AHO、POH和关节固定畸形的中国男孩。对GNAS-Gsα进行测序分析发现,该男孩及其母亲存在杂合的C.432+2T>C(P.?)变体(NM_000516.7),影响第5内含子的典型剪接供体位点,表明存在GNAS突变的母系遗传。该患者被诊断为POH重叠综合征(POH/PHP 1a)。补充钙和骨化三醇后,他的癫痫发作次数减少,并进行了手术以纠正由HO引起的关节固定畸形。本病例报告为POH重叠综合征的基因型-表型相关性提供了有价值的见解,并强调了基因检测在诊断罕见疾病中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a2f/11282909/76a67e1857be/j_biol-2022-0918-fig001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验