Search results
Results from the WOW.Com Content Network
Hair-grooming syncope (also known as hair-combing syncope) is a form of syncope (a fainting disorder) associated with combing and brushing one's hair. It is most typically seen in children aged five to sixteen. Hair-grooming syncope typically manifests as presyncopal symptoms during hair combing, brushing, braiding, trimming, curling or blow ...
Other types of hair loss that can affect hair growth around your crown include: Alopecia areata , a form of immune system-related hair loss that involves damage to your hair follicles.
Hallermann–Streiff syndrome is a congenital disorder that affects growth, cranial development, hair-growth, and dental development. There are fewer than 200 people with the syndrome worldwide. [ citation needed ] One notable organization that is supporting people with Hallermann–Streiff syndrome is the Germany-based "Schattenkinder e.V".
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 .
A child with a double crown. A cowlick is a section of human hair that stands straight up or lies at an angle at odds with the style in which the rest of an individual's hair is worn. [1] [2] The most common site of a human cowlick is in the crown, but they can appear anywhere on the head. They also sometimes occur in the front and back of the ...
Similarly, in German it is called Weichselzopf, or Vistula braid, zopf meaning a braid, and the Vistula being a river in Poland. Initially, the plait was considered an amulet to keep illness away from the body, as it was believed that when disease resolved it left the body to live in the hair, resulting in lessened suffering. For this reason ...
Acro–dermato–ungual–lacrimal–tooth syndrome (ADULT syndrome) is a rare genetic disease. [1] It is an autosomal dominant form of ectodermal dysplasia, a group of disorders that affects the hair, teeth, nails, sweat glands, and extremities. [2] The syndrome arises from a mutation in the TP63 gene. [3]
Although it tends to regress naturally later in childhood, there is no definitive treatment for Uncombable Hair Syndrome. The only recommended treatment is using soft brushes and gentle conditioners. It is also recommended to avoid hair treatments that can be harsh on hair (excessive brushing, blow drying, perms, or coloring hair).