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低钙性佝偻病的遗传形式。

Genetic Forms of Calciopenic Rickets.

作者信息

Donmez Ayse Sena, Turkyilmaz Ayberk, Cayir Atilla

机构信息

Department of Pediatrics, Regional Training and Research Hospital, Erzurum, Turkey.

Department of Medical Genetics, Karadeniz Technical University Faculty of Medicine, Trabzon, Turkey.

出版信息

Eurasian J Med. 2022 Dec;54(Suppl1):159-163. doi: 10.5152/eurasianjmed.2022.22322.

Abstract

Rickets is a disease involving calcium and phosphate balance disturbances in the pediatric population. A series of hereditary disorders known as vitamin D-dependent rickets are defined as early-onset rickets resulting from either an insufficient response to active vitamin D or an inability to maintain adequate levels of the active forms of vitamin D. According to the age at onset and the pathophysiology of the disease, various clinical signs including growth failure, limb bowing, and joint enlargement may be present. Vitamin D-dependent rickets type 1A, type 1B, type 2A, type 2B, and type 3 are classified as genetic forms. Further studies are crucial for the development of targeted therapies and future mutation-specific therapies.

摘要

佝偻病是一种涉及儿童群体钙和磷平衡紊乱的疾病。一系列被称为维生素D依赖性佝偻病的遗传性疾病被定义为早发性佝偻病,其病因要么是对活性维生素D反应不足,要么是无法维持足够水平的活性维生素D形式。根据发病年龄和疾病的病理生理学,可能会出现各种临床症状,包括生长发育迟缓、肢体弯曲和关节肿大。1A型、1B型、2A型、2B型和3型维生素D依赖性佝偻病被归类为遗传形式。进一步的研究对于开发靶向治疗和未来的突变特异性治疗至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba51/11163336/75db14b8ead2/eajm-54-S1-S159_f001.jpg

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