Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 417 for babies
  1. Sudden infant death with dysgenesis of the testes syndrome 
    Sudden infant death with dysgenesis of the testes syndrome (SIDDT) is a rare condition that is fatal in the first year of life; its major features include abnormalities ...
    https://medlineplus.gov/...th-with-dysgenesis-of-the-testes-syndrome - Genetics
  2. Hereditary hyperekplexia 
    Hereditary hyperekplexia is a condition in which affected infants have increased muscle tone (hypertonia) and an exaggerated ... stimuli, especially loud noises. Following the startle reaction, infants experience a brief period in which they are ...
    https://medlineplus.gov/genetics/condition/hereditary-hyperekplexia - Genetics
  3. Lamellar ichthyosis 
    ... is a condition that mainly affects the skin. Infants with this condition are typically born with a ... life, and then it becomes obvious that affected babies have scaly skin, and eyelids and lips that ...
    https://medlineplus.gov/genetics/condition/lamellar-ichthyosis - Genetics
  4. Harlequin ichthyosis 
    ... a severe genetic disorder that affects the skin. Infants with this condition are born prematurely with very ... lead to breathing difficulties and respiratory failure in babies with harlequin ichthyosis. Affected infants also have feeding ...
    https://medlineplus.gov/genetics/condition/harlequin-ichthyosis - Genetics
  5. Nonsyndromic aplasia cutis congenita 
    ... aplasia cutis congenita is a condition in which babies are born with localized areas of missing skin ( ... the skin defect are also underdeveloped.Most affected babies have a single lesion. The lesions vary in ...
    https://medlineplus.gov/.../nonsyndromic-aplasia-cutis-congenita - Genetics
  6. Caffey disease 
    ... a bone disorder that most often occurs in babies. Excessive new bone formation (hyperostosis) is characteristic of ... lower legs (tibia and fibula) become fused together. Babies with Caffey disease also have swelling of joints ...
    https://medlineplus.gov/genetics/condition/caffey-disease - Genetics
  7. Autosomal recessive primary microcephaly 
    ... microcephaly primary hereditary") is a condition in which infants are born with a very small head and ... comes from the Greek words for "small head."Infants with MCPH have an unusually small head circumference ...
    https://medlineplus.gov/.../autosomal-recessive-primary-microcephaly - Genetics
  8. Congenital hypothyroidism 
    ... function of the thyroid gland (hypothyroidism) that affects infants from birth (congenital). The thyroid gland is a ... result from the shortage of thyroid hormones. Affected babies may show no features of the condition, although ...
    https://medlineplus.gov/genetics/condition/congenital-hypothyroidism - Genetics
  9. Amish lethal microcephaly 
    Amish lethal microcephaly is a disorder in which infants are born with a very small head and underdeveloped brain.Infants with Amish lethal microcephaly have a sloping forehead ...
    https://medlineplus.gov/genetics/condition/amish-lethal-microcephaly - Genetics
  10. 6q24-related transient neonatal diabetes mellitus 
    ... is a type of diabetes that occurs in infants. This form of diabetes is characterized by high ... growth before birth (severe intrauterine growth retardation). Affected infants have hyperglycemia and an excessive loss of fluids ( ...
    https://medlineplus.gov/...ated-transient-neonatal-diabetes-mellitus - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next