نتایج جستجو برای: aphallia

تعداد نتایج: 31  

2014
Sasi Kumar

Aphallia or Penile agenesis is a rare urogenital anomaly with an estimated incidence of 1 in 30 million. We report a case of aphallia in a male, who had two well-developed testicles, but lacked a penis. An earlier goal of treatment for such presentations was female gender reassignment and feminizing reconstruction of perineum, more recent goal

2016
Fereshteh Talebpour Amiri Davood Nasiry Zarrin Ghabaee Ramezan Ali Naeimi Seyed Javad Seyedi Seyed Abdollah Mousavi

BACKGROUND Aphallia or penile agenesis is a rare malformation accompanying with no phallus. This anomaly is extremely rare with abnormality of urogenital system and psychological consequences. Its outbreak is estimated 1 out of 10-30 million births. CASE Reviewing 3 cases of male external genitalia agenesis, which associated with multiple anomalies of musculoskeletal, cardiovascular and genit...

2015
Deepak Sharma Ravinder Singh Sweta Shastri

Aphallia (absence of penis) is an extremely rare abnormality which has rarely been described in medical literature and can be part of the urorectal septum malformation sequence (URSMS). URSMS has hardly been reported in medical literature and includes the absence of perineal and anal openings in association with ambiguous genitalia and urogenital, colonic, and lumbosacral anomalies. This case r...

Journal: :Archives of Iranian medicine 2015
Saeid Aslanabadi Sina Zarrintan Habib Abdollahi Reza Rikhtegar Samad Beheshtirouy Davoud Badebarin Mohamed A Baky Fahmy

Aphallia or penile agenesis is an extremely rare congenital anomaly with an estimated incidence rate of 1 in 10 to 30 million births. We report a rare case of aphallia with right kidney hypoplasia and left kidney dysplasia in a 10-day old Iranian-Azeri male. The patient had creatinine rise and renal failure due to dysplastic left kidney and hypoplastic right kidney and expired on fifth day of a...

2014
Rahul Gupta Shyam Bihari Sharma Girish Prabhakar Jitendra Prasad Bhatnagar

Congenital aphallia or penile agenesis is a complex urogenital malformation and an extremely rare condition in the medical literature with reported incidence of 1 in 30 million live births. The condition is apparent at birth and is almost never missed. Objectives behind the study were to present the management and solve the dilemma with congenital aphallia. We present a retrospective study of t...

Journal: :Journal of Evolution of Medical and Dental Sciences 2014

Journal: :Asian journal of andrology 2011
Giulio Garaffa Amr Abdel Raheem David John Ralph

Penile reconstruction still represents a formidable challenge for the urologist. In this review, the most recent advances in penile reconstruction after trauma, excision of benign and malignant disease and in patients with micropenis, aphallia or female to male gender dysphoria are reported.

موسوی, سید عبداله, نخشب, مریم,

Aphallia or complete absence of penis is an extremely rare genitourinary anomaly derived from a faulty development of the genital tubercle during embryonic life. It usually coexists with other congenital anomalies. This anomaly has a very significant psychosocial impact on the child and parents. We describe herewith a neonate with male genotype who presented with aphallia and multiple anomalies...

Journal: :Journal of pediatric urology 2016
Diego Estevam Gomes Oliveira Marcela Leal da Cruz Riberto Liguori Gilmar Garrone Bruno Leslie Sérgio Leite Ottoni Geórgia Rubiane Souza Valdemar Ortiz Roberto de Castro Antonio Macedo

OBJECTIVE Aphallia 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. MATERIALS AND METHODS We performed a Pubmed search using the terms: neophalloplasty, neophallus, and phalloplasty, and selected articles that presented technical alter...

اصل زارع, محمد, شمسا, علی, مورخ, محمد, پریزاده, محمد جواد,

Introduction: Aphallia is a very rare urogenital anomaly with incidence rate of 1 in 30,000,000. It usually coexists with other anomalies such as cardiovascular anomalies which are incompatible with normal life, and therefore infants are delivered stillbirth or live for a very short period of time. Methods: We present an 18 months old boy with aphallia associated with congenital urethrorectal ...

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