Hemiscrotal agenesis: a novel phenotype of a rare malformation.

doi:10.1186/s12887-020-02424-y

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Article

Hemiscrotal agenesis: a novel phenotype of a rare malformation.

BMC pediatrics - 28 Nov 2020

Mansy Mohamed, Kotb Mostafa, Abdelmeguid Yasmine, Raafat Shaymaa, Abdelaziz Marwa

Abstract excerpt

BACKGROUND: Hemiscrotal agenesis (HSA) is an exceedingly rare congenital anomaly in scrotal development. It is characterized by unilateral absence of scrotal skin with intact midline raphe. In the English literature, only seven patients were diagnosed with HSA. Herein, we report a 14-month-old boy with HSA, unilateral cryptorchidism and a perineal skin tag. Additionally, the patient had a monodactylous limb,...

Topics

Cryptorchidism
Humans
Infant
Male
Perineum
Phenotype
Scrotum

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Identifiers

PMID: 33248450
DOI: 10.1186/s12887-020-02424-y
PMCID: PMC7697378

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