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Results 1 - 10 of 824 for means syndrome
  1. Guillain-Barré syndrome 
    ... inheriting a genetic variation linked with Guillain-Barré syndrome does not mean that a person will develop the condition. Acute infectious polyneuritis Acute inflammatory polyneuropathy Fisher syndrome GBS Guillain-Barre syndrome Landry-Guillain-Barre syndrome ...
    https://medlineplus.gov/genetics/condition/guillain-barre-syndrome - Genetics
  2. Beckwith-Wiedemann syndrome 
    ... the body. It is classified as an overgrowth syndrome, which means that affected infants are larger than normal (macrosomia), and some may be taller than their peers during childhood. Growth begins to slow by about ... syndrome, specific body parts may grow abnormally large on ...
    https://medlineplus.gov/.../condition/beckwith-wiedemann-syndrome - Genetics
  3. Simpson-Golabi-Behmel syndrome 
    ... males. This condition is classified as an overgrowth syndrome, which means that affected infants are considerably larger than normal at birth (macrosomia) and continue to grow and gain weight at an unusual rate. The other ... syndrome vary widely. People with mild cases often live ...
    https://medlineplus.gov/.../condition/simpson-golabi-behmel-syndrome - Genetics
  4. GPC3 gene 
    ... syndrome. This condition is classified as an overgrowth syndrome, which means that affected infants are considerably larger than normal at birth (macrosomia) and continue to grow and gain weight at an unusual ... cause Simpson-Golabi-Behmel syndrome delete part or all of the GPC3 gene, ...
    https://medlineplus.gov/genetics/gene/gpc3 - Genetics
  5. Isolated Duane retraction syndrome 
    ... 70 percent of all cases of Duane retraction syndrome are isolated, which means they occur without other signs and symptoms. The remaining cases of Duane retraction syndrome occur as part of syndromes that affect other ...
    https://medlineplus.gov/.../isolated-duane-retraction-syndrome - Genetics
  6. Russell-Silver syndrome 
    ... 11 chromosome 7 Most cases of Russell-Silver syndrome are sporadic, which means they occur in people with no history of the disorder in their family.Rarely, Russell-Silver syndrome can run in families. In some affected families, ...
    https://medlineplus.gov/genetics/condition/russell-silver-syndrome - Genetics
  7. Congenital hemidysplasia with ichthyosiform erythroderma and limb defects 
    ... to cause the condition.Most cases of CHILD syndrome occur sporadically, which means only one member of a family is affected. Rarely, the condition can run in families and is passed from mother to ... CHILD syndrome occurs almost exclusively in females because affected males ...
    https://medlineplus.gov/...hthyosiform-erythroderma-and-limb-defects - Genetics
  8. Sturge-Weber syndrome 
    ... mutation that causes this disorder is somatic, which means it occurs after conception. In Sturge-Weber syndrome, the mutation is thought to occur in a ...
    https://medlineplus.gov/genetics/condition/sturge-weber-syndrome - Genetics
  9. Lennox-Gastaut syndrome 
    ... ALG13 DNM1 GABRB3 Most cases of Lennox-Gastaut syndrome are sporadic, which means they occur in people with no history of the disorder in their family. When Lennox-Gastaut syndrome is associated with a genetic change, the variant ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  10. Craniofrontonasal syndrome 
    ... in about half the body's cells. This means that in affected females with craniofrontonasal syndrome, the X chromosome with an EFNB1 gene mutation ...
    https://medlineplus.gov/.../condition/craniofrontonasal-syndrome - Genetics
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