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Pan Afr Med J ; 42: 251, 2022.
Artigo em Francês | MEDLINE | ID: mdl-36338557

RESUMO

Encephalocele is a malformation due to a defect in the closure of the neural tube causing herniation of brain tissue and/or meninges through this congenital skull defect. The size of encephalocele varies from a few centimeters to a huge mass called "giant encephalocele". Content usually consists of degenerative neural tissue, meninges and a cystic part. We here report the case of a 4-month-old infant, born of non-consanguineous parents, who was referred with congenital occipital mass. Upon arrival at our clinic, clinical examination revealed a weight of 3500g, a head circumference of 33 cm, with a non-bulging anterior fontanelle. She presented with a huge renitent occipital mass measuring 43X25cm, with a height of 15cm was found. absence of both eyelids, bilateral lip and palate fissures; a constriction ring on the right leg, absence of toes on the right and left feet. A diagnosis of an amniotic band syndrome was made, with as components: occipital encephalocele associated with a bilateral palpebral coloboma, a bilateral cleft lip and palate, and amniotic bands on the right leg, and amputation of the toes of the right and left feet.


Assuntos
Síndrome de Bandas Amnióticas , Fenda Labial , Fissura Palatina , Coloboma , Lactente , Recém-Nascido , Feminino , Humanos , Fenda Labial/diagnóstico , Fenda Labial/cirurgia , Fissura Palatina/diagnóstico , Fissura Palatina/cirurgia , Síndrome de Bandas Amnióticas/diagnóstico , Encefalocele/diagnóstico , Encefalocele/cirurgia , Coloboma/complicações , Perna (Membro) , Universidades , Pálpebras , Dedos do Pé
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