AUTOSOMAL DOMINANT FAMILIAL HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DYSPLASIA

被引:116
|
作者
BILOUS, RW
MURTY, G
PARKINSON, DB
THAKKER, RV
COULTHARD, MG
BURN, J
MATHIAS, D
KENDALLTAYLOR, P
机构
[1] UNIV NEWCASTLE UPON TYNE,DEPT EAR NOSE & THROAT SURG,NEWCASTLE TYNE NE1 7RU,TYNE & WEAR,ENGLAND
[2] UNIV NEWCASTLE UPON TYNE,DEPT MED,NEWCASTLE TYNE NE1 7RU,TYNE & WEAR,ENGLAND
[3] UNIV NEWCASTLE UPON TYNE,DEPT PAEDIAT,NEWCASTLE TYNE NE1 7RU,TYNE & WEAR,ENGLAND
[4] UNIV NEWCASTLE UPON TYNE,DEPT HUMAN GENET,NEWCASTLE TYNE NE1 7RU,TYNE & WEAR,ENGLAND
[5] MRC,CLIN RES CTR,DIV MOLEC MED,HARROW HA1 3UJ,MIDDX,ENGLAND
来源
NEW ENGLAND JOURNAL OF MEDICINE | 1992年 / 327卷 / 15期
关键词
D O I
10.1056/NEJM199210083271506
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
FAMILIAL hypoparathyroidism is an unusual condition that can present at any time from early infancy until well into adulthood.1 2 3 4 It can be inherited in an autosomal dominant,3 , 4 autosomal recessive,5 or X-linked recessive6 , 7 pattern. Its presence has been associated with other congenital abnormalities, such as absence of the thymus (DiGeorge's syndrome).8 We recently encountered a patient with long-standing sensorineural deafness who presented with symptoms of thirst and polyuria and was found to have diabetes mellitus. He also had hypocalcemia, subsequently proved to be due to hypoparathyroidism, and a high serum creatinine concentration; further studies revealed small kidneys with a large right-sided… © 1992, Massachusetts Medical Society. All rights reserved.
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收藏
页码:1069 / 1074
页数:6
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