De las bases embriológicas a la clínica en el síndrome de Prune Belly / From the embryological basis to the clinical Prune Belly syndrome
Rev. cuba. obstet. ginecol
;
42(2): 254-259, abr.-jun. 2016. ilus, graf
Article
in Spanish
| LILACS
| ID: lil-797746
RESUMEN
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(AU)
ABSTRACT
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(AU)
Full text:
Available
Index:
LILACS (Americas)
Main subject:
Prune Belly Syndrome
Type of study:
Diagnostic study
/
Prognostic study
Limits:
Female
/
Humans
/
Male
/
Infant, Newborn
Language:
Spanish
Journal:
Rev. cuba. obstet. ginecol
Journal subject:
Gynecology
/
Obstetrics
Year:
2016
Type:
Article
Affiliation country:
Colombia
Institution/Affiliation country:
Universidad Icesi/CO
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