Familial hypomagnesaemia with secondary hypocalcaemia: A new case that indicates autosomal recessive inheritance

Journal of Inherited Metabolic Disease

Volumn 24, Issue 8, 2001, Pages 875-876

  Meyer, P ^a,b   Boettger, M B ^b  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b Human Resources Inc   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BICARBONATE; CALCIUM; COLECALCIFEROL; MAGNESIUM; VITAMIN D;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BLOOD GAS ANALYSIS; CASE REPORT; FEMALE; HUMAN; HYPOCALCEMIA; HYPOMAGNESEMIA; MALE; METABOLIC ACIDOSIS; SIBLING; X CHROMOSOME RECESSIVE DISORDER;

ADOLESCENT; ADULT; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; GENES, RECESSIVE; HUMANS; HYPOCALCEMIA; MAGNESIUM; MAGNESIUM DEFICIENCY; MALE; METABOLISM, INBORN ERRORS;

EID: 0035722701     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1013952510698     Document Type: Article

References (3)

1. Primary infantile hypomagnesaemia; report of two cases and review of literature
2. Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: Mapping of the Xp22 chromosome breakpoint
3. Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: Genetic linkage mapping and analysis of a balanced translocation breakpoint