A Rare Observation of Brachymetacarpia and Brachymetatarsia in a Patient with Primary Idiopathic Hypoparathyroidism.

IF 0.9 Q4 ENDOCRINOLOGY & METABOLISM
Parackrama Karunathilake, Arun Rajaratnam, W K S Kularatne
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Abstract

Brachymetacarpia and brachymetatarsia are unique clinical entities associated with numerous rare conditions. Primary hypoparathyroidism is distinct from pseudohypoparathyroidism and pseudopseudohypoparathyroidism by lacking skeletal changes such as short metacarpals or metatarsals. Here, we present a case of a 64-year-old patient with brachymetacarpia and brachymetatarsia presented with hypocalcemic symptoms and signs, bilateral cataracts, and basal ganglia calcifications, subsequently diagnosed with idiopathic primary hypoparathyroidism. This is a rare case describing such an infrequent observation of brachymetacarpia and brachymetatarsia in primary idiopathic hypoparathyroidism.

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原发性特发性甲状旁腺功能减退症患者掌跖不足和跖不足的罕见观察。
掌心短视和跖骨短视是一种罕见的临床疾病。原发性甲状旁腺功能减退症不同于假性甲状旁腺功能减退症和假性甲状旁腺功能减退症,其特征是缺乏短掌骨或跖骨等骨骼变化。在此,我们报告一例64岁的近跖骨和近跖骨畸形患者,其表现为低钙症状和体征、双侧白内障和基底节区钙化,随后被诊断为特发性原发性甲状旁腺功能低下。这是一个罕见的病例,描述了原发性特发性甲状旁腺功能减退症中不常见的跖骨短促和跖骨短促。
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来源期刊
Case Reports in Endocrinology
Case Reports in Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
2.10
自引率
0.00%
发文量
45
审稿时长
13 weeks
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