Department of Medicine and Therapeutics, University of Ghana Medical School, Ghana.
Department of Medicine and Therapeutics, Korle Bu Teaching Hospital, Ghana.
West Afr J Med. 2023 Oct 31;40(10):1131-1134.
Parathyroid hormone (PTH) resistance, the main biochemical feature of a rare group of disorders known as Pseudohypoparathyroidism (PHP) is an uncommon cause of hypocalcaemia. In addition to the biochemical abnormalities, some individuals with PHP may have features of Albright Hereditary Osteodystrophy (AHO). Being a rare disorder with a significant level of variation and overlap in its clinical presentation, diagnosis of PHP may be challenging in some clinical settings. This case report highlights the diagnosis of this rare disorder.
A 20-year-old Ghanaian female who had been involved in a road traffic accident (RTA) was referred to the endocrine clinic after a computer tomography (CT) scan of her head revealed an incidental finding of multiple basal ganglia calcifications. Investigations revealed hypocalcaemia, hyperphosphatemia, and elevated intact PTH in the presence of normal levels of 25-hydroxyvitamin D and magnesium, and a normal kidney function. She also had phenotypic features of AHO. Findings suggested a diagnosis of PHP, however, the type could not be identified due to the unavailability of further testing.
This report of a Ghanaian female with PTH resistance and features of AHO diagnosed at the age of 20 years, is expected to add to the existing literature and assist in increasing the level of awareness and facilitate the diagnosis of this disorder in our setting.
甲状旁腺激素(PTH)抵抗是一种罕见的疾病群,称为假性甲状旁腺功能减退症(PHP)的主要生化特征,是低钙血症的一个不常见原因。除了生化异常外,一些 PHP 患者可能具有 Albright 遗传性骨营养不良症(AHO)的特征。由于这是一种罕见的疾病,其临床表现存在显著的变异和重叠,因此在某些临床环境下诊断 PHP 可能具有挑战性。本病例报告强调了这种罕见疾病的诊断。
一名 20 岁的加纳女性,在一次道路交通事故(RTA)中受伤,头部 CT 扫描发现多发性基底节钙化的意外发现后被转介到内分泌科诊所。检查显示低钙血症、高磷血症和完整的 PTH 升高,同时 25-羟维生素 D 和镁水平正常,肾功能正常。她也有 AHO 的表型特征。检查结果提示诊断为 PHP,但由于缺乏进一步的检测,无法确定其类型。
本报告介绍了一名加纳女性,20 岁时患有 PTH 抵抗和 AHO 特征,预计将增加现有文献,并有助于提高我们环境中的认识水平,促进这种疾病的诊断。