A rare presentation: Penile agenesis, vesicoureteral reflux, and rectovesical fistula in a newborn [PDF]
The penis is an important organ in fertility, urinary and psychosexual structure of males. Complete penile agenesis is a rare congenital genitourinary anomaly and is usually associated with other malformations such as gastrointestinal, cardiac, and ...
Müslim Yurtçu
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Penile agenesis associated with anorectal malformation and bilateral renal agenesis: A case report and a review of the literature [PDF]
Penile agenesis is complete absence of the penis in an otherwise normal phenotypic and genotypic male at birth that results from failure of development of the genital tubercle.
Collins Chijioke Adumah +9 more
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Penile agenesis is an extremely rare disorder with profound urological and psychological consequences. The goal of treatment is an early female gender assignment and feminizing reconstruction of the perineum.
Bangroo A, Khetri Ramji, Tiwari Sashi
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This rare congenital znomaly had been reported in only 37 cases The condition is a result of incomplete development of the genital tubercle. Other urogenital anomaly should be investigated thoroughly.
I. J. Gupta, Ramesh Chandra
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Penile agenesis: a case report
Penile agenesis is a rarely seen congenital anomaly with dramatic psychological outcomes. In more than half of the patients, other genitourinary anomalies can accompany penile agenesis.
Nuriye Tarakçı +2 more
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Aphallia (Penile agenesis): A preliminary report of three cases
Aphallia (penile agenesis) is an extremely rare abnormality with the reported incidence of 1 in 30 million births. The cause of this anomaly is associated with no genital tubercle formation or its development impairment. The majority of patients have 46XY Karyotype. The scrotum, testes and testicular function are usually normal.
Prashant Sadashiv Patil +6 more
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PENILE AGENESIS-ADOLESCENCE PRESENTATION. [PDF]
Sharma GP, Verma BS.
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Penile agenesis (afallia) in pueros
Introduction. Penile agenesis (aphallia) is an extremely rare congenital defect characterized by the complete absence of the penis in a child with a male karyotype 46XY.Material. The analysis of the literature on keywords in the Pubmed and Medline databases was carried out.Results.
И. М. Каганцов +4 more
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22q11 deletion syndrome and urogenital manifestationsA clinicopathological case report and review of the literatureM.Vachette MD*, GE.Grant MD*, J.Bouquet de Joliniere MD.PhD*, M. Jotterand MD** N.Ben Ali MD*, A.Feki MD.PhD * and R.Brugger MD.*Department of gynecology and obstetrics, HFR, Fribourg, Switzerland.** Institute of pathology, CHUV, Lausanne, Switzerland. [PDF]
Background: Deletion in the chromosomal region 22q11 results from the abnormal development of the third and fourth pharyngeal pouches during embryonic life and presents an expansive phenotype with more than 180 clinical features described that involve ...
Jean Bouquet De Jolinière
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De Castro falloplasty of the with penile agenesis
Introduction. Penile agenesis (aphallia) is an extremely rare congenital disorder. At present, about 100 cases of the anomaly have been described around the world. The incidence of this congenital anomaly is estimated to be one case per 2030 million births.
И. М. Каганцов +2 more
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