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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.
Hypertrichosis cubiti is characterized by an unusually high concentration of longhairs that are concentrated mostly in the elbow area on the extensor surfaces of the upper extremities. Hypertrichosis is not always visible at birth; it typically manifests in early infancy, peaks between the ages of 5 and 6, then gradually declines and eventually ...
Hypertrichosis is often mistakenly classified as hirsutism. [1] Hirsutism is a type of hypertrichosis exclusive to women and children, resulting from an excess of androgen-sensitive hair growth. [16] Patients with hirsutism exhibit patterns of adult male hair growth. [1] Chest and back hair are often present on women with hirsutism. [16]
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 ...
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 ...
X-linked hypertrichosis, also known as X-linked congenital generalized hypertrichosis, is a hereditary disorders characterized by generalized congenital hypertrichosis and thick eyebrows. [ 1 ] Signs and symptoms
Nevoid hypertrichosis is a rare disorder characterized by a confined patch of coarse terminal hair. [2] It often manifests at or shortly after birth, [3] while it sporadically manifests later in life. [4] The lesion is known to stay stable, and the child's growth is directly correlated with any size rise. [2]
Barber-Say syndrome (BSS) is a very rare congenital disorder associated with excessive hair growth (hypertrichosis), fragile skin, eyelid deformities , and an overly broad mouth (macrostomia). [ 1 ] Barber-Say syndrome is phenotypically similar to Ablepharon macrostomia syndrome , which is also associated with dominant mutations in TWIST2 .