Results 1 to 10 of about 189 (101)

Aphallia: A Rare Congenital Anomaly in a Low-Resource Setting [PDF]

open access: yesInternational Medical Case Reports Journal, 2023
Awet Ghebreberhan Mehretab,1,* Nahom Daniel Berhe,2,* Emnet Tekeste Fekadu3 1Department of Surgery, Adi Quala Hospital, Adi Quala, Eritrea; 2Department of Internal Medicine, Mendefera Zonal Referral Hospital, Mendefera, Eritrea; 3Department of ...
Awet Ghebreberhan Mehretab
exaly   +6 more sources

A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula [PDF]

open access: yesRadiology Case Reports, 2022
Aphallia or penile agenesis is a rare case of the genitourinary system which has an association with upper urinary tract disorder. Failure of fetal genital tubercle formation in the embryonic period is the cause of this disorder.
Saeid Esmaeilian   +2 more
exaly   +4 more sources

Congenital lack of penis – aphallia [PDF]

open access: yesBMC Pediatrics
Aphallia is a term that means lack of penis. It is a rare congenital anomaly in which the penis does not develop during the embryonic period 1. In this condition, the opening of the urethra is not located in the typical place.
Dimitar Dachev   +3 more
doaj   +4 more sources

Aphallia - congenital absence of the penis: a systematic review [PDF]

open access: yesBMC Urology
Background Aphallia is a rare congenital anomaly often associated with other urogenital anomalies. The management of aphallia cases for both the immediate and long-term treatment of patients with aphallia pose a major dilemma.
Prahara Yuri   +4 more
doaj   +4 more sources

Aphallia in a patient with 9q34 duplication syndrome: a case report [PDF]

open access: yesBMC Urology
Introduction Congenital aphallia is a rare condition with less than 100 documented cases. It may occur isolated or in association with additional anomalies such as gastrointestinal malformations, caudal defects, imperforate anus, and other genitourinary ...
Juan Pablo Meza-Espinoza   +9 more
doaj   +4 more sources

Isolated aphallia: a case report and review of literature

open access: yesAfrican Journal of Urology, 2023
Background Aphallia is a rarest of rare congenital anomaly the incidence being 1 in 10 to 30 million live births. Seen at birth, it leaves the parents and family disturbed.
Siddharth Sathaye, Ulhas Sathaye
exaly   +3 more sources

Aphallia: Report of three cases and literature review [PDF]

open access: yesIranian Journal of Reproductive Medicine, 2016
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.
Davood Nasiry Zarrin Ghabaee   +4 more
doaj   +5 more sources

A case report of aphallia with urorectal septum malformation sequence in a newborn: a very rarely seen condition [PDF]

open access: yesInternational Medical Case Reports Journal, 2015
Deepak Sharma,1 Ravinder Singh,2 Sweta Shastri3 1Department of Neonatology, Fernandez Hospital, Hyderabad, 2Department of Pediatrics, Civil Hospital, Hisar, Haryana, 3Department of Pathology, NKP Salve Medical College, Nagpur, Maharashtra, India ...
Ravinder Singh
exaly   +4 more sources

Phalloplasty in Complete Aphallia and Ambiguous Genitalia [PDF]

open access: yesSeminars in Plastic Surgery, 2011
The most common indications for phalloplasty in children include aphallia, micropenis/severe penile inadequacy, ambiguous genitalia, phallic inadequacy associated with epispadias/bladder exstrophy and female to male gender reassignment in adolescents.
Richard Redett, Rachel Bluebond-Langner
exaly   +5 more sources

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

open access: yesInternational Medical Case Reports Journal, 2023
Tigabu Daniel,1 Yonas Abera2 1Surgery Department, Hawassa University, Hawassa, Ethiopia; 2Surgery Department, Ethiopian Defense University, Addis Ababa, EthiopiaCorrespondence: Tigabu Daniel, Email danieltigabu96@gmail.comBackground: Aphallia (absent ...
Daniel T, Abera Y
doaj   +2 more sources

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