From the embryological basis to the clinical prune belly syndrome
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Pachajoa Londoño, Harry Mauricio
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Editorial Ciencias Medicas
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Resumen
Prune Belly syndrome is a congenital disorder that is due, as currently reported, to genetic basis. It is characterized by the following triad: deficiency of abdominal muscles in varying degrees, bilateral cryptorchidism and urinary tract anomalies. Two variants of the syndrome are identified, a deadly one and another compatible with life. © 2016, Editorial Ciencias Medicas. All rights reserved.
Description
El síndrome de Prune Belly es un trastorno congénito, que obedece según lo
reportado actualmente a una base genética. Está caracterizado por la siguiente
triada: deficiencia en grados variables de la musculatura abdominal, criptorquidia
bilateral y anomalías del tracto urinario. Se identifican dos variantes del síndrome,
una mortal y otra compatible con la vida.
Palabras clave
Trastornos genéticosEnfermedades RarasAnomalías congénitasSíndrome Prune BellyCiencias socio biomédicas
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Except where otherwised noted, this item's license is described as Atribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)