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- Megalencephaly abstract "Megalencephaly (or Macrencephaly abbreviated MEG) is a growth development disorder in which the brain is abnormally large. It is characterized by a brain with an average weight that is 2.5 standard deviations from the mean of the general population. Megalencephaly is usually diagnosed at birth and is confirmed with an MRI. A mutation in the PI3K-AKT pathway is believed to be the primary cause of brain proliferation and ultimately the root cause of megalencephaly. This mutation has produced a classification of brain overdevelopment that consists of two syndromes including, megalencephaly-capillary malformation (MCAP) and megalencephaly-polydactyly-polymicrogyria-hydrocephalus (MPPH). Approximately 1 out of 50 children (2%) are said to have the characteristics of megalencephaly in the general population. There are several neuropsychiatric disorders linked with megalencephaly, however, studies have shown that autism is the most prevalent association with the malformation of MEG. Although no treatment currently exists for megalencephaly, management methods are focused at reducing deficits linked with autism. Most recent research is targeted at creating inhibitors to reduce the mutational pathway that causes megalencephaly.".
- Megalencephaly diseasesdb "22519".
- Megalencephaly icd10 "Q04.5".
- Megalencephaly icd9 "742.4".
- Megalencephaly omim "155350".
- Megalencephaly wikiPageID "232049".
- Megalencephaly wikiPageRevisionID "592466077".
- Megalencephaly diseasesdb "22519".
- Megalencephaly hasPhotoCollection Megalencephaly.
- Megalencephaly icd "742.4".
- Megalencephaly icd "Q04.5".
- Megalencephaly name "Megalencephaly".
- Megalencephaly omim "155350".
- Megalencephaly wordnet_type synset-disease-noun-1.
- Megalencephaly subject Category:Congenital_disorders_of_nervous_system.
- Megalencephaly type Abnormality114501726.
- Megalencephaly type Abstraction100002137.
- Megalencephaly type Anomaly114505821.
- Megalencephaly type Attribute100024264.
- Megalencephaly type BirthDefect114465048.
- Megalencephaly type Condition113920835.
- Megalencephaly type CongenitalDisordersOfNervousSystem.
- Megalencephaly type Defect114464005.
- Megalencephaly type Disease114070360.
- Megalencephaly type IllHealth114052046.
- Megalencephaly type Illness114061805.
- Megalencephaly type Imperfection114462666.
- Megalencephaly type PathologicalState114051917.
- Megalencephaly type PhysicalCondition114034177.
- Megalencephaly type State100024720.
- Megalencephaly type Disease.
- Megalencephaly type AilmentCondition.
- Megalencephaly type Situation.
- Megalencephaly comment "Megalencephaly (or Macrencephaly abbreviated MEG) is a growth development disorder in which the brain is abnormally large. It is characterized by a brain with an average weight that is 2.5 standard deviations from the mean of the general population. Megalencephaly is usually diagnosed at birth and is confirmed with an MRI. A mutation in the PI3K-AKT pathway is believed to be the primary cause of brain proliferation and ultimately the root cause of megalencephaly.".
- Megalencephaly label "Megalencephaly".
- Megalencephaly label "Megaloencefalia".
- Megalencephaly label "Megaloencefalia".
- Megalencephaly sameAs Megaloencefalia.
- Megalencephaly sameAs Megaloencefalia.
- Megalencephaly sameAs m.01hr9x.
- Megalencephaly sameAs Q10748814.
- Megalencephaly sameAs Q10748814.
- Megalencephaly sameAs Megalencephaly.
- Megalencephaly wasDerivedFrom Megalencephaly?oldid=592466077.
- Megalencephaly isPrimaryTopicOf Megalencephaly.
- Megalencephaly name "Megalencephaly".