نتایج جستجو برای: هیپوپاراتیروییدیسم hypoparathyroidism

تعداد نتایج: 1759  

Journal: :The Journal of clinical endocrinology and metabolism 2004
Olga Kifor Aidan McElduff Meryl S LeBoff Francis D Moore Robert Butters Ping Gao Thomas L Cantor Imre Kifor Edward M Brown

Autoimmune hypoparathyroidism is thought to result from immune-mediated destruction of the parathyroid glands. We encountered two patients with hypoparathyroidism and other autoimmune conditions (Graves' disease and Addison's disease, respectively) in whom autoimmune destruction of the parathyroid glands had not taken place. In the first, a histologically normal parathyroid gland was observed a...

2014
Evelyn Ning Man Cheung Susan R George Gary A Costain Danielle M Andrade Eva W C Chow Candice K Silversides Anne S Bassett

BACKGROUND 22q11.2 deletion syndrome (22q11.2DS) is a relatively common yet under-recognized genetic syndrome that may present with endocrine features. We aimed to address the factors that contribute to the high prevalence of hypocalcaemia. METHODS We investigated hypocalcaemia in a well-characterized sample of 138 adults with 22q11.2DS (65 m, 73 F; mean age 34.2, SD 11.8, years) using labora...

Journal: :Human molecular genetics 2007
Asif Ali Paul T Christie Irina V Grigorieva Brian Harding Hilde Van Esch S Faisal Ahmed Maria Bitner-Glindzicz Eberhard Blind Catherine Bloch Patricia Christin Peter Clayton Jozef Gecz Brigitte Gilbert-Dussardier Encarna Guillen-Navarro Anna Hackett Isil Halac Geoffrey N Hendy Fiona Lalloo Christoph J Mache Zulf Mughal Albert C M Ong Choni Rinat Nicholas Shaw Sarah F Smithson John Tolmie Jacques Weill M Andrew Nesbit Rajesh V Thakker

The hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome is an autosomal dominant disorder caused by mutations of the dual zinc finger transcription factor, GATA3. We investigated 21 HDR probands and 14 patients with isolated hypoparathyroidism for GATA3 abnormalities. Thirteen different heterozygous germline mutations were identified in patients with HDR. These consisted of three nonsens...

2008
Ichiro Miyata Hideki Yoshikawa Naokiyo Kurokawa Kei-ichi Kanno Yoshihiro Hayashi Yoshikatsu Eto

We experienced a case of familial hypoparathyroidism with an autosomal dominant pattern of transmission and performed molecular analysis of the calcium-sensing receptor (CASR) gene. The patient was a female neonate, born by cesarean section at term because of breech presentation. Her mother had been diagnosed with idiopathic hypoparathyroidism at the age of 9 yr and had been receiving vitamin D...

Journal: :European journal of endocrinology 1998
T Watanabe H Mochizuki N Kohda K Minamitani M Minagawa T Yasuda H Niimi

OBJECTIVE A family is described which has a unique combination of autosomal dominant hypoparathyroidism and sensorineural deafness without renal dysplasia. CASE REPORT The proband was a male infant aged 1 month with episodes of seizures for 20 days. He was born at 35 weeks' gestation without asphyxia, weighing 2040 g. His initial calcium, phosphorus and percentage of tubular reabsorption of p...

2016
Yousuke Higuchi Kosei Hasegawa Miho Yamashita Yousuke Fujii Hiroyuki Tanaka Hirokazu Tsukahara

BACKGROUND Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disorder. We report the first detailed case of hypoparathyroidism complicated by biliary atresia. CASE PRESENTATION A 1-year-old Japanese girl was admitted to our hospital for living donor liver transplantation. She suffered from obstructive jaundice owing to biliary atresia. She...

2016
Anastasia Gkampeta Eftyxia Kouma Anastasia Touliopoulou Efstathios Aggelopoulos Eleni Vourti

© 2016 Journal of Neurosciences in Rural Practice | Published by Wolters Kluwer Medknow Hypocalcemia is rare in childhood and caused, among other conditions, by hypoparathyroidism. DiGeorge syndrome is the most common cause of hypoparathyroidism in childhood. Presentation of a rare cause of hypocalcemia in childhood and the necessity of measuring serum electrolyte levels in patients presenting ...

Journal: :BMJ Case Reports 2015

Journal: :The Kurume Medical Journal 1975

Journal: :Arquivos Brasileiros de Endocrinologia & Metabologia 2006

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