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Beckwith-Wiedemann syndrome: A case report / Philippine Journal of Obstetrics and Gynecology
Philippine Journal of Obstetrics and Gynecology ; : 88-95, 2011.
Article Dans Anglais | WPRIM | ID: wpr-732066
ABSTRACT
Beckwith-Wiedemann Syndrome (BWS) is a rare congenital overgrowth disorder due to alterations in specific genes in chromosome 11p15. It has a variable clinical picture. Infants may exhibit a combination of the following characteristics macroglossia, macrosomia, abdominal wall defects, ear creases or posterior helical pits, hypoglycemia, polyhydramnios and prematurity. Presented is a case of a 24-year-old gravida 3 para 2 (2002) who manifested with preterm labor and polyhydramnios. She delivered a preterm live baby girl who was diagnosed to have Beckwith-Wiedemann syndrome. The rarity of this condition, as well as the significant maternal and perinatal complications associated with it, is discussed in this paper.
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Syndrome de Beckwith-Wiedemann / Macrosomie foetale / Chromosomes / Polyhydramnios / Paroi abdominale / Hypertrophie / Hypoglycémie / Macroglossie Limites du sujet: Adulte / Femelle / Humains / Grossesse langue: Anglais Texte intégral: Philippine Journal of Obstetrics and Gynecology Année: 2011 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Syndrome de Beckwith-Wiedemann / Macrosomie foetale / Chromosomes / Polyhydramnios / Paroi abdominale / Hypertrophie / Hypoglycémie / Macroglossie Limites du sujet: Adulte / Femelle / Humains / Grossesse langue: Anglais Texte intégral: Philippine Journal of Obstetrics and Gynecology Année: 2011 Type: Article