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X-Linked Recessive form of Nephrogenic Diabetes Insipidus in a 7-Year-Old Boy.
Janchevska, A; Tasic, V; Gucev, Z; Krstevska-Konstantinova, M; Cheong, H I.
Afiliação
  • Janchevska A; University Children's Hospital Skopje, Medical Faculty, Skopje, Macedonia.
  • Tasic V; University Children's Hospital Skopje, Medical Faculty, Skopje, Macedonia.
  • Gucev Z; University Children's Hospital Skopje, Medical Faculty, Skopje, Macedonia.
  • Krstevska-Konstantinova M; University Children's Hospital Skopje, Medical Faculty, Skopje, Macedonia.
  • Cheong HI; Seoul National University Children's Hospital, Seoul, Korea ; Research Coordination Center for Rare Diseases, Seoul National University Hospital, Seoul, Korea ; Kidney Research Institute, Medical Research Center, Seoul National University College of Medicine, Seoul, Korea.
Balkan J Med Genet ; 17(2): 81-5, 2014 Dec.
Article em En | MEDLINE | ID: mdl-25937802
Nephrogenic diabetes insipidus (NDI) is caused by the inability of renal collecting duct cells to respond to arginine vasopressin (AVP)/antidiuretic hormone (ADH). We present the case of a 7-year-old boy with a history of excretion of large amounts of dilute urine and polydipsia since infancy. The boy had several vomiting episodes with mild dehydration during the first 3 years of life. There was no evidence of headaches, dizziness or visual problems. He drinks between 2 and 3 L/day and has 24-hour diuresis of 2 liters, now. He has prepubertal appearance with appropriate weight [+0.85 standard deviation score (SDS)] and height (+0.15 SDS) for his age. His intelligence was also normal. The water deprivation test showed low urine osmolality after 8 hours of dehydration. After desmopressin administration, urine osmolality remained low. Serum osmolality was in the normal range for sex and age before and after desmopressin administration. This indicated a nephrogenic form of diabetes insipidus. Molecular analyses revealed a P286L [p.Pro(CCC)286Leu(CTC)] mutation in the AVPR2 gene, that was inherited from his mother. This patient is the first case with genetically confirmed X-linked inherited form of NDI in the Republic of Macedonia. Molecular analysis confirmed the clinical diagnosis and enabled genetic advice for this family.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2014 Tipo de documento: Article