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Korean Journal of Perinatology ; : 56-60, 1999.
Article in Korean | WPRIM | ID: wpr-14808

ABSTRACT

Holoprosencephaly is a rare and complex malformation affecting the cleavage of the developing forebrain and is usually associated with defects of the mid Face. We have experienced a case of holoprosencephaly, diagnosed prenatally by ultrasound examination at 31 weeks of pregnancy in a 31-year-old primigravida woman. This case is characterized by holoprosencephaly, cleft palate, cleft lip, left renal aplasia and right renal hypertrophy. The chromosomal study showed a deletion of the long arm of chromosome 7, 46, XX, del(7)(q32), We report with a terminal deletion of chromosome 7q associated with atypical clinical picture and holoprosencephaly.


Subject(s)
Adult , Female , Humans , Pregnancy , Arm , Chromosome Aberrations , Chromosomes, Human, Pair 7 , Cleft Lip , Cleft Palate , Holoprosencephaly , Hypertrophy , Multicystic Dysplastic Kidney , Prosencephalon , Ultrasonography
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