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Results 1 - 10 of 41 for plus
  1. Genetic epilepsy with febrile seizures plus (GEFS+) is a spectrum of seizure disorders of varying severity. GEFS+ is usually diagnosed in families whose members have a combination ...
  2. Coats plus syndrome is an inherited condition characterized by an eye disorder called Coats disease plus abnormalities of the brain, bones, gastrointestinal system, and ...
  3. Peters plus syndrome is an inherited condition that is characterized by eye abnormalities, short stature, an opening in the ... and intellectual disability.The eye problems in Peters plus syndrome occur in an area at the front ...
  4. Histiocytosis-lymphadenopathy plus syndrome (also known as SLC29A3 spectrum disorder) is a group of conditions with overlapping signs and symptoms that ... tract.This spectrum is known as histiocytosis-lymphadenopathy plus syndrome because the disorders that make up the ...
  5. ... chorea and spastic paraplegia Iraqi Jewish optic atrophy plus MGA, type III MGA3 OPA3 defect Optic atrophy plus syndrome Genetic Testing Registry: 3-Methylglutaconic aciduria type ...
  6. ... of the condition. Deafness and myopia Deafness, cochlear, plus DFNMYP High myopia and sensorineural deafness High myopia- ...
  7. ... Citation on PubMed Asmus F, Gasser T. Dystonia-plus syndromes. Eur J Neurol. 2010 Jul;17 Suppl ...
  8. ... types. At least 10 mutations that cause Peters plus syndrome have been identified in the B3GLCT gene. Peters plus syndrome is characterized by eye abnormalities, short stature, ...
  9. ... gene have been identified in people with Coats plus syndrome. This disorder is characterized by an eye condition called Coats disease plus abnormalities of the brain, bones, gastrointestinal system, and ...
  10. ... found to cause genetic epilepsy with febrile seizures plus (GEFS+), which is a spectrum of seizure disorders ... usually stop by age 5, and febrile seizures plus (FS+). FS+ involves febrile and other types of ...
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