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Results 1 - 10 of 43 for Abnormality of the scalp hair
  1. SMARCA2 gene 
    ... Baraitser syndrome. This condition is characterized by multiple abnormalities, primarily sparse scalp hair, small head size (microcephaly), distinctive facial features, short ...
    https://medlineplus.gov/genetics/gene/smarca2 - Genetics
  2. Cantú syndrome 
    ... distinctive facial appearance, heart defects, and several other abnormalities. The features of the disorder vary among affected individuals.People with Cantú syndrome have thick scalp hair that extends onto the forehead and grows down ...
    https://medlineplus.gov/genetics/condition/cantu-syndrome - Genetics
  3. Naegeli-Franceschetti-Jadassohn syndrome/dermatopathia pigmentosa reticularis 
    ... sweat (hypohidrosis) or excess sweating (hyperhidrosis) and dental abnormalities. Some affected individuals also have hair loss (alopecia) on the scalp, eyebrows, and underarms. The alopecia is described as ...
    https://medlineplus.gov/...rome-dermatopathia-pigmentosa-reticularis - Genetics
  4. Netherton syndrome 
    ... invaginata. In addition to the hair on the scalp, the eyelashes and eyebrows may be affected. The hair abnormality in Netherton syndrome may not be noticed in ...
    https://medlineplus.gov/genetics/condition/netherton-syndrome - Genetics
  5. Incontinentia pigmenti 
    ... signs and symptoms of incontinentia pigmenti can include hair loss (alopecia) on the scalp and other parts of the body, dental abnormalities (such as small teeth or few teeth), and ...
    https://medlineplus.gov/genetics/condition/incontinentia-pigmenti - Genetics
  6. Clouston syndrome 
    ... sweat glands. Specifically, Clouston syndrome is characterized by abnormalities of the hair, nails, and skin, with the teeth and sweat glands being unaffected.In infants with Clouston syndrome, scalp hair is sparse, patchy, and lighter in color ...
    https://medlineplus.gov/genetics/condition/clouston-syndrome - Genetics
  7. Anhidrotic ectodermal dysplasia with immune deficiency 
    ... with this condition survive only into childhood.Skin abnormalities in children with EDA-ID include areas that are dry, wrinkled, or darker in color than the surrounding skin. Affected individuals tend to have sparse scalp and body hair (hypotrichosis). EDA-ID is also characterized by missing ...
    https://medlineplus.gov/...todermal-dysplasia-with-immune-deficiency - Genetics
  8. X-linked chondrodysplasia punctata 2 
    ... atrophoderma). Most affected individuals also have sparse, coarse hair on their scalps.Most people with X-linked chondrodysplasia punctata 2 have clouding of the lens of the eye (cataracts) from birth or early childhood. Other eye abnormalities that have been associated with this disorder include ...
    https://medlineplus.gov/.../x-linked-chondrodysplasia-punctata-2 - Genetics
  9. Focal dermal hypoplasia 
    ... individuals may have small, ridged fingernails and toenails. Hair on the scalp can be sparse and brittle or absent.Many individuals with focal dermal hypoplasia have hand and foot abnormalities, including missing fingers or toes (oligodactyly), webbed or ...
    https://medlineplus.gov/genetics/condition/focal-dermal-hypoplasia - Genetics
  10. Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome 
    ... throughout childhood and into adulthood, frequently affecting the scalp, neck, hands, and feet. Skin erosion ranges from mild to severe and can lead to life-threatening infection in infancy, scarring, and hair loss. Other ectodermal abnormalities in AEC syndrome include changes in skin coloring; ...
    https://medlineplus.gov/...odermal-defects-cleft-lip-palate-syndrome - Genetics
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