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Results 1 - 10 of 16 for Dry hair
  1. Uncombable hair syndrome 
    ... syndrome is a condition that is characterized by dry, frizzy hair that cannot be combed flat. This condition develops in childhood, often between infancy and age ...
    https://medlineplus.gov/genetics/condition/uncombable-hair-syndrome - Genetics
  2. Cardiofaciocutaneous syndrome 
    ... with cardiofaciocutaneous syndrome also tend to have thin, dry, curly hair and sparse or absent eyelashes and eyebrows.Infants ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  3. Autosomal recessive hypotrichosis 
    ... beginning in infancy. This hair is usually coarse, dry, and tightly curled (often described as woolly hair). Scalp hair may also be lighter in color ...
    https://medlineplus.gov/.../autosomal-recessive-hypotrichosis - Genetics
  4. Multiple sulfatase deficiency 
    ... developmental delay, and slow growth. They also have dry, scaly skin (ichthyosis) and excess hair growth (hypertrichosis). Skeletal abnormalities can include abnormal side- ...
    https://medlineplus.gov/.../condition/multiple-sulfatase-deficiency - Genetics
  5. Keratoderma with woolly hair 
    ... these conditions have hair that is unusually coarse, dry, fine, and tightly curled. In some cases, the hair is also sparse. The woolly hair texture typically ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  6. Giant congenital melanocytic nevus 
    ... time. The skin of the nevus is often dry and prone to irritation and itching (dermatitis). Excessive hair growth (hypertrichosis) can occur within the nevus. There ...
    https://medlineplus.gov/.../giant-congenital-melanocytic-nevus - Genetics
  7. Hashimoto's disease 
    ... tiredness (fatigue), weight gain or difficulty losing weight, hair that is thin and dry, a slow heart rate, joint or muscle pain, ...
    https://medlineplus.gov/genetics/condition/hashimotos-disease - Genetics
  8. Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy 
    ... inflammation (hepatitis), lung irritation (pneumonitis), dry mouth and dry eyes (Sjogren-like syndrome), inflammation of the eyes (keratitis), kidney problems (nephritis), vitamin B12 deficiency, hair loss (alopecia), loss of skin color in blotches ( ...
    https://medlineplus.gov/...inopathy-candidiasis-ectodermal-dystrophy - Genetics
  9. Anhidrotic ectodermal dysplasia with immune deficiency 
    ... 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
  10. X-linked chondrodysplasia punctata 2 
    ... X-linked chondrodysplasia punctata 2 are born with dry, scaly patches of skin (ichthyosis) in a linear or spiral (whorled) pattern. The scaly patches fade over time, leaving abnormally colored blotches of skin without hair (follicular atrophoderma). Most affected individuals also have sparse, ...
    https://medlineplus.gov/.../x-linked-chondrodysplasia-punctata-2 - Genetics
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