Results 91 to 100 of about 232 (115)
Aphallia: Its Classification and Management
Journal of Urology, 1989 Aphallia is an extremely rare disorder with profound urological and psychological consequences. Approximately 60 patients have been reported on in the literature; we report our experience with 3 additional patients. Fifty patients had sufficient information to classify the condition according to the site of the urethral meatus.
S J, Skoog, A B, Belman
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Pediatric Surgery International, 2007
Aphallia is a rare genital anomaly poorly reported in literature. The authors describe an atypical case of aphallia characterized by ultrasound and magnetic resonance imaging findings of atrophic cavernous corpus associated with anterior urethral opening.
Kathia Chaumoitre +2 more
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Aphallia is a rare genital anomaly poorly reported in literature. The authors describe an atypical case of aphallia characterized by ultrasound and magnetic resonance imaging findings of atrophic cavernous corpus associated with anterior urethral opening.
Kathia Chaumoitre +2 more
exaly +3 more sources
Aphallia: experience with 3 cases
Journal of Pediatric Surgery, 2010In view of the rarity of the lesion, we describe 3 cases of aphallia associated with genitourinary and nongenitourinary anomalies. One case was associated with an anorectal malformation, whereas 2 had a normal anal opening. One patient with a normal anal opening had an associated rectal-urethro-fistula. Development of the phallus, clinical presentation
Manish Pathak
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Neophalloplasty in boys with aphallia: A systematic review
Journal of Pediatric Urology, 2016Aphallia is a rare penile congenital abnormality. The aim of this systematic review was to assess all available literature on neophalloplasty in infancy with an interest in technical alternatives and clinical outcome.We performed a Pubmed search using the terms: neophalloplasty, neophallus, and phalloplasty, and selected articles that presented ...
Marcela Leal Da Cruz +2 more
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Phalloplasty in complete aphallia: pedicled anterolateral thigh flap
Journal of Plastic, Reconstructive and Aesthetic Surgery, 2009A phalloplasty using the pedicled anterolateral thigh flap in three patients with aphallia is described. The technique, its advantages and disadvantages are discussed.
Donald Hudson
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Aphallia, Its Classification and Management
Journal of Urology, 1987 Steven J. Skoog
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Aphallia as part of urorectal septum malformation sequence in an infant of a diabetic mother
American Journal of Medical Genetics, Part A, 1999 A male patient with aphallia, anal stenosis, tetralogy of Fallot, multiple vertebral anomalies including sacral agenesis and central nervous system (CNS) malformations was born after a pregnancy complicated by poorly controlled maternal diabetes ...
Karen Gripp +2 more
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Archives of International Surgery, 2015
Aphallia or penile agenesis is complete absence of the penis due to complete or partial failure in the phallic development of the genital tubercle. It is a rare form of genital ambiguity with an estimated incidence of 1 in 10-30 million births and
NishithM Paul Ekka +3 more
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Aphallia or penile agenesis is complete absence of the penis due to complete or partial failure in the phallic development of the genital tubercle. It is a rare form of genital ambiguity with an estimated incidence of 1 in 10-30 million births and
NishithM Paul Ekka +3 more
openaire +1 more source
Aphallia: Case report and review of the literature
Saudi Surgical Journal, 2015Aphallia or absence of the penis is a very rare congenital anomaly with an estimated incidence of 1 in 10,000,000 births. A total of about 80 cases have been documented so far. We present a case of 1-day neonate who was born preterm at 30 weeks by normal vaginal delivery with a birth weight of 1.9 kg.
Nameer Faiz, Amarendra Kumar
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Hinyokika kiyo. Acta urologica Japonica, 1997
We report a case of aphallia in a male neonate. The phallus was completely absent. The urethral meatus was located between the well developed bifid scrotum containing normal testes. Voiding cystourethrography revealed grade II VUR on the right side. The karyotype was 46XY. Other urogenital anomalies were not detected.
N, Nakaigawa +3 more
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We report a case of aphallia in a male neonate. The phallus was completely absent. The urethral meatus was located between the well developed bifid scrotum containing normal testes. Voiding cystourethrography revealed grade II VUR on the right side. The karyotype was 46XY. Other urogenital anomalies were not detected.
N, Nakaigawa +3 more
openaire +1 more source