Results 11 to 20 of about 232 (115)

A New Presentation: Aphallia, Vesicoureteral Reflux, Rectovesical Fistula, and Adrenal Insufficiency [PDF]

open access: yesCase Reports in Pediatrics, 2020
Aphallia or penile agenesis is a rare congenital malformation with an estimated incidence rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated anomalies including caudal axis, cardiovascular, genitourinary, and ...
R. El Qadiry   +4 more
doaj   +3 more sources

Aphallia Associated with Anorectal Malformation. [PDF]

open access: yesSultan Qaboos Univ Med J, 2022
NONE
Blachman-Braun R   +4 more
europepmc   +6 more sources

Aphallia: A case report and literature review

open access: yesAfrican Journal of Paediatric Surgery, 2011
Aphallia is a complex urogenital malformation. It is rarely described in literature. Treatment calls upon feminising genitoplasty in most cases. Authors describe a case in a neonate, insisting on the sociocultural realities which guided their indications.
A D Kane, G Ngom, O Ndour, D M Alumeti
doaj   +6 more sources

Penile Reconstruction in Aphallia: Modification of the De Castro Technique With Large Tissue Expander [PDF]

open access: yesPlastic and Reconstructive Surgery, Global Open
Summary:. Aphallia is an exceedingly rare congenital malformation. The condition is the result of a sporadic anatomic anomaly during fetal development in a 46, XY male patient with otherwise normal functioning testes and male sexual hormone metabolism ...
Joanna Chen, BA   +7 more
doaj   +3 more sources

Male gender assignment of a child with aphallia and associated complex urological anomaly [PDF]

open access: yesJournal of Indian Association of Pediatric Surgeons, 2017
A 2-year-old male child presented to us with aphallia. At birth, he was passing urine from the anus and had undergone emergency colostomy and pyelostomy for urinary sepsis at 1 week of life.
Satish Kumar Kolar Venkatesh   +3 more
doaj   +3 more sources

An Extremely Rare Case Report of Aphallia with Horseshoe Kidney and Ureterohydronephrosis [Letter] [PDF]

open access: yesInternational Medical Case Reports Journal
Verónica Judith Picos-Cárdenas,1 Evelia Leal-Ugarte,2 Juan Pablo Meza-Espinoza2 1Laboratorio de Genética, Facultad de Medicina, Universidad Autónoma de Sinaloa, Culiacán, Sinaloa, C. P.
Picos-Cárdenas VJ   +2 more
doaj   +4 more sources

Scrotal phalloplasty: A novel surgical technique for aphallia during infancy and childhood by pre-anal anterior coronal approach [PDF]

open access: yesJournal of Indian Association of Pediatric Surgeons, 2012
All the currently known reconstructions for aphallia are carried out around puberty. We describe a novel technique as a temporizing procedure which would see the patient through childhood.
Minu Bajpai
doaj   +3 more sources

Clinical Image of Aphallia: A Rare Congenital Anomaly [PDF]

open access: yesJournal of Clinical and Diagnostic Research
A six-year-old boy with a karyotype of 46XY presented to the outpatient department with congenital absence of the penis, known as aphallia (Table/Fig 1).
Aditya Sriharsha Pedaprolu   +1 more
doaj   +3 more sources

"Bird-Wing" abdominal phalloplasty: A novel surgical technique for penile reconstruction [PDF]

open access: yesJournal of Indian Association of Pediatric Surgeons, 2013
Aim: To describe a technique of phalloplasty that is devoid of donor site scarring and suitable for urethral inlay and penile prosthesis in subsequent stages in cases of aphallia.
Minu Bajpai
doaj   +3 more sources

Aphallia with urethrorectal fistula, bladder and urethral calculi

open access: yesMajallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, 2006
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 ...
M Movarrekh   +3 more
doaj   +2 more sources

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