Pseudohypoparathyroidism: a rare but important cause of hypocalcaemia.
نویسندگان
چکیده
We present a 46-year-old Caucasian lady with symptomatic hypocalcaemia. Investigations revealed markedly raised parathyroid hormone (PTH) levels with vitamin D deficiency. A number of conditions causing secondary hyperparathyroidism were ruled out from her medical history and initial investigations. The main differential diagnoses were vitamin D deficiency and PTH resistance (pseudohypoparathyroidism, PHP). With high-normal serum phosphate and normal alkaline phosphatase, and a lack of symptoms associated with osteomalacia, vitamin D deficiency alone was unlikely to be the cause of hypocalcaemia. Given a normal physical appearance, genetic testing was arranged and confirmed the diagnosis of PHP type Ib. She is currently taking activated vitamin D to maintain calcium homeostasis. PTH resistance is the hallmark of PHP, a rare complex genetic disorder, which can be easily missed resulting in potentially serious consequences.
منابع مشابه
Pseudohypoparathyroidism, rare cause of hypocalcaemia!
Pseudohypoparathyroidism is a rare disorder which is characterized by end organ parathormone resistance, which causes hypocalcaemia, hyperphosphataemia and high parathormone levels. We are reporting here case of a young male who had symptoms of chronic hypocalcaemia, with a positive Trousseau's and Chvostek's sign on examination, without any features of Albright's hereditary osteodystrophy. Lab...
متن کاملAin't No Sunshine When She's Gone: Pseudohypoparathyroidism Discovered in an Adult
An 18-year-old negroid woman presented with progressive cramps in both hands. She was Jamaican and had moved to The Netherlands 8 months before. On physical examination Trousseau's sign was positive. Laboratory analysis showed severe hypocalcaemia (1.17 mmol/L) and hyperphosphatemia (2.0 mmol/L). Urinary excretion of both calcium (0.8 mmol/day) and phosphate (5 mmol/day) was low, as is seen in ...
متن کاملNeurological, Electroencephalographic, and Heredo-famillal Aspects of Pseudohypoparathyroidism and Pseudo-pseudohypoparathyroidism*
The Neurology and Medical Departments of the Detroit Receiving Hospital have recently made clinical and electroencephalographic (E.E.G.) studies of two patients in a family in which several members appear to have either pseudohypoparathyroidism or pseudo-pseudohypoparathyroidism. The findings were of sufficient interest to prompt us to review this subject and to present our findings since the n...
متن کاملJ . Neurol . Neurosurg . Psychiat . , 1960 , 23 , 33 . NEUROLOGICAL , ELECTROENCEPHALOGRAPHIC , AND HEREDO - FAMILLAL ASPECTS OF PSEUDOHYPOPARATHYROIDISM AND PSEUDO - PSEUDOHYPOPARATHYROIDISM
The Neurology and Medical Departments of the Detroit Receiving Hospital have recently made clinical and electroencephalographic (E.E.G.) studies of two patients in a family in which several members appear to have either pseudohypoparathyroidism or pseudo-pseudohypoparathyroidism. The findings were of sufficient interest to prompt us to review this subject and to present our findings since the n...
متن کاملNeurological, electroencephalographic, and heredo-familial aspects of pseudohypoparathyroidism and pseudopseudohypoparathyroidism. J.
The Neurology and Medical Departments of the Detroit Receiving Hospital have recently made clinical and electroencephalographic (E.E.G.) studies of two patients in a family in which several members appear to have either pseudohypoparathyroidism or pseudo-pseudohypoparathyroidism. The findings were of sufficient interest to prompt us to review this subject and to present our findings since the n...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- BMJ case reports
دوره 2013 شماره
صفحات -
تاریخ انتشار 2013