Familial hypomagnesemia hypercalciuria [manz syndrome]
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2006; 16 (6): 428-430
in English
| IMEMR
| ID: emr-77460
ABSTRACT
We report a case of a rare inherited tubular disorder of linked transport of magnesium and calcium at the level of ascending limb of loop of Henle, characterized by hypomagnesemia, hypercalciuria and nephrocalcinosis, known as "Manz syndrome" who presented with polyuria, nystagmus and recurrent episodes of tetany with radiological evidence of rickets and nephrocalcinosis
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Syndrome
/
Gitelman Syndrome
/
Hypercalciuria
/
Magnesium
/
Nephrocalcinosis
Type of study:
Case report
Limits:
Humans
/
Male
Language:
English
Journal:
J. Coll. Physicians Surg. Pak.
Year:
2006
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