Familial idiopathic hypoparathyroidism, sensorineural deafness and renal dysplasia

被引:6
作者
Ishida, S [1 ]
Isotani, H [1 ]
Kameoka, K [1 ]
Kishi, T [1 ]
机构
[1] Hirakata City Hosp, Dept Internal Med, Hirakata, Osaka 5731013, Japan
关键词
PTH; abdominal CT; audiogram; genetic mutation;
D O I
10.2169/internalmedicine.40.110
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We describe a 27-year-old woman with familial idiopathic hypoparathyroidism, bilateral sensorineural deafness and right renal aplasia, There was a family history of deafness in her father and two other family members with sensorineural deafness, one of whom had hypoparathyroidism, To our knowledge, there have been four previous reports of idiopathic hypoparathyroidism associated with sensorineural deafness and renal dysplasia, The clinical features were not identical to any of the four previous reports. Although no chromosome abnormalities were present in the patient using standard trypsin G-handing analysis, we speculate that some common genetic mutation caused hypoparathyroidism, sensorineural deafness and renal dysplasia.
引用
收藏
页码:110 / 113
页数:4
相关论文
共 17 条
[1]   MUTATION OF THE SIGNAL PEPTIDE-ENCODING REGION OF THE PREPROPARATHYROID HORMONE GENE IN FAMILIAL ISOLATED HYPOPARATHYROIDISM [J].
ARNOLD, A ;
HORST, SA ;
GARDELLA, TJ ;
BABA, H ;
LEVINE, MA ;
KRONENBERG, HM .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (04) :1084-1087
[2]   FAMILIAL NEPHROSIS, NERVE DEAFNESS, AND HYPOPARATHYROIDISM [J].
BARAKAT, AY ;
DALBORA, JB ;
MARTIN, MM ;
JOSE, PA .
JOURNAL OF PEDIATRICS, 1977, 91 (01) :61-64
[3]   AUTOSOMAL DOMINANT FAMILIAL HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DYSPLASIA [J].
BILOUS, RW ;
MURTY, G ;
PARKINSON, DB ;
THAKKER, RV ;
COULTHARD, MG ;
BURN, J ;
MATHIAS, D ;
KENDALLTAYLOR, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (15) :1069-1074
[4]   AUTOSOMAL OR X-LINKED RECESSIVE SYNDROME OF CONGENITAL LYMPHEDEMA, HYPOPARATHYROIDISM, NEPHROPATHY, PROLAPSING MITRAL-VALVE, AND BRACHYTELEPHALANGY [J].
DAHLBERG, PJ ;
BORER, WZ ;
NEWCOMER, KL ;
YUTUC, WR .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 16 (01) :99-104
[5]   KENNY-CAFFEY SYNDROME IN 2 SIBS BORN TO CONSANGUINEOUS PARENTS - EVIDENCE FOR AN AUTOSOMAL RECESSIVE VARIANT [J].
FRANCESCHINI, P ;
TESTA, A ;
BOGETTI, G ;
GIRARDO, E ;
GUALA, A ;
LOPEZBELL, G ;
BUZIO, G ;
FERRARIO, E ;
PICCATO, E .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 42 (01) :112-116
[6]  
Hasegawa T, 1997, AM J MED GENET, V73, P416, DOI 10.1002/(SICI)1096-8628(19971231)73:4<416::AID-AJMG9>3.0.CO
[7]  
2-L
[8]   COMBINED PITUITARY STIMULATION TEST - INTERACTIONS OF HYPOTHALAMIC RELEASING HORMONES IN MAN [J].
HOLL, RW ;
LOOS, U ;
HETZEL, WD ;
HEINZE, E ;
FEHM, HL .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1988, 11 (03) :219-223
[9]   Hypoparathyroidism and insulin-dependent diabetes mellitus in a patient with Kearns-Sayre syndrome harbouring a mitochondrial DNA deletion [J].
Isotani, H ;
Fukumoto, Y ;
Kawamura, H ;
Furukawa, K ;
Ohsawa, N ;
Goto, Y ;
Nishino, I ;
Nonaka, I .
CLINICAL ENDOCRINOLOGY, 1996, 45 (05) :637-641
[10]  
Isotani H, 1995, Nihon Naibunpi Gakkai Zasshi, V71, P65