Micropenis is a medical term that describes an unusually small penis in a human male. A common criterion is a dorsal penile length at least 2.5 standard deviations smaller than the mean penis size; if penis length follows a normal distribution, about 0.6% of penises will be in the micropenis category.
The condition is usually recognized shortly after birth, when the stretched flaccid penis of a full-term infant boy measures less than 1.9 cm from base to tip. The term is most often used medically when the rest of the penis, scrotum, and perineum is well-formed, without ambiguity such as hypospadias.
Micropenis can have a variety of causes. Since it is defined statistically, a large proportion of males with micropenis are simply normal but in the lowest percentile of normal size. As for many other conditions, the term "idiopathic" is often used when a cause cannot be determined.
Of the abnormal conditions associated with micropenis, most are conditions of reduced prenatal androgen production or effect. Examples include abnormal testicular development (testicular dysgenesis, Klinefelter syndrome, Leydig cell hypoplasia), specific defects of testosterone or dihydrotestosterone synthesis (17,20-lyase deficiency, 5α-reductase deficiency), androgen insensitivity syndromes, inadequate pituitary stimulation (gonadotropin deficiency) or other forms of congenital hypogonadism. Micropenis can also occur as part of many genetic malformation syndromes not involving the sex chromosomes. It sometimes is a sign of congenital growth hormone deficiency or congenital hypopituitarism. Finally, several Homeobox genes have been identified which affects penis and digit size without detectable hormone abnormalities.
Pediatric endocrinologists are usually the physicians to whom these boys are referred. After evaluation to detect any of the conditions described above, micropenis can often be treated in infancy with injections of various hormones, such as human chorionic gonadotropin or testosterone.
Most eight to fourteen year old boys referred for micropenis have
A high incidence of micropenis has been found in several Asian populations, including Japanese, Chinese (of varying ethnicity) and Vietnamese samples, considered due to a higher mutation rate for the SRD5A2 gene, which encodes for the enzyme 5{alpha}-reductase-2 and plays a role in male sex differentiation (Sasaki et al. 2003). The mutation led to decreased expression of the enzyme, which in turn results in penises with erect lengths of -2.5 standard deviations. In the case of the Japanese sample, hormone treatments were also studied and found to be effective, resulting in penis lengths at nearly the average of age-matched Japanese controls.
In extreme cases of micropenis, there is barely any shaft, and the glans appears to sit almost on the pubic skin. From the 1960s until the late 1970s, it was not unusual for sex reassignment and surgery to be recommended. This was especially likely if evidence suggested that response to additional testosterone and pubertal testosterone would be poor. If parents accepted, the boy would be reassigned and renamed as a girl, and surgery performed to remove the testes and construct an artificial vagina. This was based on three now questioned assumptions:
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