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Results 1 - 10 of 456 for Infancy
  1. Malignant migrating partial seizures of infancy 
    Malignant migrating partial seizures of infancy (MMPSI) is a severe form of epilepsy that begins very early in life. Recurrent seizures begin before the age of ...
    https://medlineplus.gov/...ant-migrating-partial-seizures-of-infancy - Genetics
  2. Generalized arterial calcification of infancy 
    Generalized arterial calcification of infancy (GACI) is a disorder affecting the circulatory system that becomes apparent before birth or within the first few months ...
    https://medlineplus.gov/...ralized-arterial-calcification-of-infancy - Genetics
  3. STING-associated vasculopathy with onset in infancy 
    STING-associated vasculopathy with onset in infancy (SAVI) is a disorder involving abnormal inflammation throughout the body, especially in the skin, blood vessels, and lungs. Inflammation normally occurs when ...
    https://medlineplus.gov/...ciated-vasculopathy-with-onset-in-infancy - Genetics
  4. Trichohepatoenteric syndrome 
    ... Intractable diarrhea with phenotypic anomalies Phenotypic diarrhea of infancy SD/THE Syndromic diarrhea THE syndrome THES Tricho- ... Goulet O, Badens C. Syndromic (phenotypic) diarrhoea of infancy/tricho-hepato-enteric syndrome. Arch Dis Child. 2014 ...
    https://medlineplus.gov/.../condition/trichohepatoenteric-syndrome - Genetics
  5. UNC80 deficiency 
    ... problems that are apparent from birth or early infancy. The disorder does not typically get worse over ... normal size at birth but grow slowly during infancy and childhood. Unusual facial features typically occur in ...
    https://medlineplus.gov/genetics/condition/unc80-deficiency - Genetics
  6. GABA-transaminase deficiency 
    ... is a brain disease (encephalopathy) that begins in infancy. Babies with this disorder have recurrent seizures (epilepsy), ... Most do not achieve normal developmental milestones of infancy such as following others' movement with their eyes ...
    https://medlineplus.gov/.../condition/gaba-transaminase-deficiency - Genetics
  7. Pearson syndrome 
    ... is a severe disorder that usually begins in infancy. It causes problems with the development of blood- ... of children with this severe disorder die in infancy or early childhood due to severe lactic acidosis ...
    https://medlineplus.gov/genetics/condition/pearson-syndrome - Genetics
  8. ALG1-congenital disorder of glycosylation 
    ... varying signs and symptoms that typically develop during infancy and can affect several body systems.Individuals with ... often severe, with affected individuals surviving only into infancy or childhood. However, some people with this condition ...
    https://medlineplus.gov/...alg1-congenital-disorder-of-glycosylation - Genetics
  9. CDKL5 deficiency disorder 
    ... disorder is characterized by seizures that begin in infancy, followed by significant delays in many aspects of ... mutations as a cause of severe epilepsy in infancy: clinical and electroencephalographic long-term course in 4 ...
    https://medlineplus.gov/genetics/condition/cdkl5-deficiency-disorder - Genetics
  10. Isolated sulfite oxidase deficiency 
    ... milder, late-onset form that begins later in infancy or early childhood.Classic ISOD appears within the ... a few months. Affected individuals who survive past infancy usually develop displacement of the lenses of the ...
    https://medlineplus.gov/.../isolated-sulfite-oxidase-deficiency - Genetics
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