A rare case of alobar holoprosencephaly with normal facies.

Autor:	Singh, Prashant, Sharma, Raghavendra, Nehete, Lokesh
Předmět:	FACIAL manifestations of general diseases COUNSELING DIENCEPHALON DEVELOPMENTAL disabilities MULTIPLE human abnormalities SEVERITY of illness index SEIZURES (Medicine) PRENATAL care RARE diseases PARENTS
Zdroj:	Journal of Pediatric Neurosciences; Jan-Mar2022, Vol. 17 Issue 1, p65-67, 3p
Abstrakt:	Background: Alobar holoprosencephaly is a rare disorder of brain development. Most of the cases have facial abnormalities and the survival of such children is usually not prolonged. Case Description: We are reporting a 2-month-old female child presented with seizures and delayed developmental milestones. Interestingly, she has no facial abnormality which is quite unusual. The management of such children is difficult and individualized. Conclusion: The counseling of the parents should be done regarding the severity and outcome of such congenital disease and also the importance of the antenatal check-up during a future pregnancy. [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
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