Search results
Results From The WOW.Com Content Network
Hypertrichosis is an abnormal amount of hair growth over the body. [1] [2] The two distinct types of hypertrichosis are generalized hypertrichosis, which occurs over the entire body, and localized hypertrichosis, which is restricted to a certain area. [1] Hypertrichosis can be either congenital (present at birth) or acquired later in life.
Prepubertal hypertrichosis, also known as childhood hypertrichosis, is a cutaneous condition characterized by increased hair growth, found in otherwise healthy infants and children. [ 1 ] [ 2 ] Prepubertal hypertrichosis is a cosmetic condition and does not affect any other health aspect.
As compared with a melanocytic nevus, congenital melanocytic nevi are usually larger in diameter and may have excess terminal hair, a condition called hypertrichosis. If over 40 cm (16 in) projected adult diameter with hypertrichosis, it is sometimes called giant hairy nevus; more usually these largest forms are known as large or giant ...
Above: Lalit Patidar, a 13-year-old boy with a genetic form of hypertrichosis. "Werewolf syndrome" is generally considered a genetic condition, but in these recent cases, it was seemingly caused ...
This category contains people who have or had hypertrichosis. Pages in category "People with hypertrichosis" The following 9 pages are in this category, out of 9 total.
13-year-old Lalit Patidar from central India was given the nickname ''wolf boy'' after the effects of a rare condition, known as hypertrichosis, caused him to grow hair all over his face ...
Excessive hair growth within or on the ear is known medically as auricular hypertrichosis. [5] Some men, particularly in the male population of India, have coarse hair growth along the lower portion of the helix, a condition referred to as "having hairy pinnae" (hypertrichosis lanuginosa acquisita). [6]
Cantú syndrome is a rare condition characterized by hypertrichosis, osteochondrodysplasia, and cardiomegaly. [ 6 ] [ 5 ] Fewer than 50 cases have been described in the literature; they are associated with a mutation in the ABCC9 -gene that codes for the ABCC9-protein.