Microcephaly in a hyperphenylalaninemic infant leading to the diagnosis of maternal hyperphenylalaninemia

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Bibliographic Details
Published in:European journal of pediatrics 1996-03, Vol.155 (3), p.257-258
Main Authors: Gungor, N, Tokath, A, Coskun, T, Ozguc, M, Ozalp, I
Format: Article
Language:English
Subjects:
Consanguinity
Diagnosis
Female
Humans
Infant
Infant, Newborn
Medical diagnosis
Microcephaly
Microcephaly - diagnosis
Microcephaly - genetics
Neonatal Screening
Phenylalanine - blood
Phenylketonurias - diagnosis
Phenylketonurias - genetics
Pregnancy
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ISSN:0340-6199
1432-1076
DOI:10.1007/BF01953954