PubMed Health⌕ Search

PubMed · 10370030

Perineal-mound defects.

Abstract

Perineal-mound (PMD) and genital-fold defects cause anorectal malformations (ARM) in both sexes. They are common in females and usually present as a low anomaly (except rectovestibular fistula). They are rare in males and present as an intermediate anomaly. A common embryological explanation for these defects with varied presentation in males and females is discussed. These anomalies should be grouped separately in the classification of ARM. We present five male patients with PMD, three of whom had imperforate anus with rectobulbar fistula and perineal hypospadias and two who had imperforate anus with rectoperineal fistula.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

A K Sharma, D Goel, S K Kothari. 1999. Perineal-mound defects.. https://doi.org/10.1007/s003830050562

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Burns caused by fan heater used for managing post-operative hypothermia in a premature neonate.

Generally fan forced area heaters are considered to be incapable of causing burn injury. A case is presented where such a heater was used to prevent post-operative hypothermia after cut-back anoplasty to correct low anorectal malformation (imperforate anus) in a premature neonate. The neonate sustained dermo-epidermal (second degree) burns to the abdominal wall and right forearm which were swaddled with cloth and deep (third degree) burns to the fingers of left hand that were exposed as intravenous line was inserted at dorsum of the hand.

Anus, Imperforate↗

Shprintzen-Goldberg omphalocele syndrome: a new patient with an expanded phenotype.

Shprintzen and Goldberg [1979] described a new autosomal dominant syndrome characterized by omphalocele, scoliosis, pharyngeal and laryngeal hypoplasia, mild dysmorphic face, and learning disabilities. This condition was described in a father and three daughters, one of whom died in infancy, probably of airway narrowing. Here, we report on a second observation of this syndrome in a 6-year-old patient. In our case, omphalocele, imperforate anus, and feeding impairment were the main clinical problems in the neonatal period. Scoliosis appeared during the fourth year of age. The facial appearance is similar to the original patients and additional clinical findings are described which expand the phenotypic spectrum.

Anus, Imperforate↗