An extremely rare case of classic complete caudal duplication: Dipygus
نویسندگان
چکیده
منابع مشابه
Caudal duplication (dipygus) in a Rock Pigeon (Columba livia)
Congenital defects are those abnormalities present at birth that result from errors arising during development (Noden and de la Hunta, 1985). Congenital duplications are interesting among congenital defects because they are composed by two individuals. Multiple births most frequently result from fertilization of separately ovulated female gametes. However, complete or partial separation of clea...
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Pedunculated chorangioma is extremely rare type of chorangioma. To the best of our knowledge, no case has been reported in Indian literature. We report one such rare case in a twenty two year old primi gravida who delivered a full term live female baby by lower section caesarian section (LSCS). Gross examination revealed a nodular mass attached to the placenta by a pedicle. Histopathological ex...
متن کاملEvaluation of the lower urinary tract function in caudal duplication (dipygus) anomaly.
Caudal duplication is a rare anomaly with less than 30 reported cases. For those patients who also have double bladders, there are not enough data regarding the function of the lower urinary tract. A boy with caudal duplication anomaly was evaluated fluoroscopically and urodynamically. The results of the evaluation showed that the bladders were filling and emptying synchronously with normal and...
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Urethralduplication is a rare condition occurs as a congenital malformation either independently or in the setting of other congenital malformations such as caudal duplication syndrome. Its prevalence becomes even rarer if it manifests as two side-by-side tracts in coronal plan.Nonetheless, we introduce a unique presentation of complete coronal urethral duplication accompanied by astoundin...
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Acalvaria defined as absent skull bones, is an extremely rare congenital anomaly with only a handful of cases reported in literature. In this report we presented a male newborn case of acalvaria referred to our hospital (Shahid Motahari hospital of Urmia, Iran). The condition per se has been described as having high mortality rate. Very few living cases, less than ten, have been reported till now.
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ژورنال
عنوان ژورنال: Journal of Indian Association of Pediatric Surgeons
سال: 2014
ISSN: 0971-9261
DOI: 10.4103/0971-9261.136478