Autor:	Dudin, K I, Teebi, A S
Zdroj:	European Journal of Pediatrics; 1987, Vol. 146 Issue 3, p303-305, 3p
Abstrakt:	A case of primary hypomagnesaemia with secondary hypocalcaemia in an Arab girl of consanguineous parents is reported. She presented at the age of 3 weeks with generalised convulsions, was treated with magnesium supplements and followed up for 5 years during which she showed normal physical and psychomotor development. In view of the striking male preponderance among the reported cases and the presence of parental consanguinity in a few, the inheritance is discussed and genetic heterogeneity is suggested. [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
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