Holoprosencephaly in neonates
| Autor: | S. P. Ram, Abdul Rahman Noor, Zahari Mahbar, T.N. Krishna |
|---|---|
| Rok vydání: | 1994 |
| Předmět: |
medicine.medical_specialty
Persistent tunica vasculosa lentis Cleft Lip Nose Single nostril Holoprosencephaly Hypotelorism medicine Humans Recurrent convulsions Craniofacial Coloboma business.industry Infant Newborn General Medicine Anatomy medicine.disease Alobar holoprosencephaly Surgery Cleft Palate Otorhinolaryngology Pediatrics Perinatology and Child Health Female medicine.symptom business Orbit Follow-Up Studies |
| Zdroj: | International Journal of Pediatric Otorhinolaryngology. 29:65-71 |
| ISSN: | 0165-5876 |
| DOI: | 10.1016/0165-5876(94)90110-4 |
| Popis: | A single nostril associated with alobar holoprosencephaly is a rare congenital lesion. This paper reports two female term neonates with holoprosencephaly. The first neonate asphyxiated at birth had a single nostril, hypotelorism, posterior cleft palate, inferonasal coloboma of the iris and disc and persistent tunica vasculosa lentis. The other neonate had cleft lip and palate and recurrent convulsions. Both neonates had gross motor and developmental delay. Cranial sonography and CT scan showed features consistent with alobar holoprosencephaly. Karyotyping for the first neonate and her family members was normal. Both of them were treated conservatively and supervised. |
| Databáze: | OpenAIRE |
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