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Perineal Hypospadias
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Perineal Hypospadias

This infant with ambiguous genitalia was a genetic male. The arrow points to the urethral orifice that opens unto the perineum.
The penile structure was without a urethra.
The testes were undescended.
(Description By:H. Yamase, M.D. )
(Image Contrib. by: UCHC )
Hypospadias
Etiology

Developmental abnormality.
There is some evidence for genetic influences; sibling of a child with hypospadias has an increased (14%) chance of having hypospadias.
Pathogenesis

Developmental malformation of the urethral groove and formation of the urethral canal.,
Epidemiology

Hypospadias is one of the more common congenital malformations, occuring in the United States at a frequency of 28.23 per 10,000 total births.
General Gross Description

Hypospadias is the abnormal location of the urethral meatus ventral to the normal glanular tip.
The urethral meatus may open on the ventral surface of the penis, at the base of the penis or the perineum.
General Microscopic Description

No specific microscopic features. Hypospadias is a gross anatomic abnormality.
Clinical Correlation

Usually does not need surgical correction.
References

Cotran RS, Kumar V, Robbins SL: Robbins Pathologic Basis of Disease. 5th ed. Philadelphia, W.B. Saunders, 1994, pp. 440 and 1007.
Neonatology, 4th edition, Avery et al. (eds), New York: Lippincott, 1994. pp. 905-906.
Hypospadias
Synopsis by: Harold Yamase M.D. (T76000M23030)[242]
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