Holoprosencephaly

Holoprosencephaly (HPE) is a complex brain malformation resulting from incomplete cleavage of the prosencephalon, occurring between the 18th and 28th day of gestation, and affecting both the forebrain and face, which results in neurological manifestations and facial anomalies of variable severity.

Hypocalcemia

An abnormally decreased calcium concentration in the blood.


Total: 2

                       


(per page)
PMID (PMCID)
16189634
 FEMALE Infant, Newborn
Hypocalcemia due to tubular dysfunction in a patient with holoprosencephaly.
Negishi M, Kano K, Shimura N, Arisaka O.
Clin Exp Nephrol. 2005;9(3):244-6.
This is the first report of a case of hypocalcemia in a female infant with holoprosencephaly.
16189634
 FEMALE Infant, Newborn
Hypocalcemia due to tubular dysfunction in a patient with holoprosencephaly.
Negishi M, Kano K, Shimura N, Arisaka O.
Clin Exp Nephrol. 2005;9(3):244-6.
Hypocalcemia due to tubular dysfunction in a patient with holoprosencephaly.