GRIN2B-related neurodevelopmental disorder

GRIN2B-related neurodevelopmental disorder is a rare neurodevelopmental disorder which is characterized by developmental delays and intellectual disabilities of variable degrees, muscle tone anomalies, feeding difficulties, and behavioral problems.[1]

GRIN2B-related neurodevelopmental disorder
Other namesGRIM2B-associated disorder
SpecialtyMedical genetics, Pediatry, Neurology
SymptomsMainly developmental delays, intellectual disabilities, craniofacial dysmorphisms, behavioural problems and muscle tone anomalies
ComplicationsLearning disability, communication delay, social ineption
Usual onsetBirth
DurationLifelong
CausesGenetic mutation
Diagnostic methodGenetic testing and physical examination
PreventionNone
PrognosisMedium
FrequencyRare, only 100 cases have been described in medical literature
Deaths-

Signs and symptoms

The following list comprises most of the symptoms people with GRIN2B show:[2][3]

Less common symptoms include:[4]

Causes

This condition is caused by mutations in the GRIN2B gene, located in chromosome 12.[5]

This gene makes instructions into how to make a protein called GluN2B, a type of NMDA receptor, which is found in brain neurons during ante-natal brain development. It is involved in correct brain development and function, regulating memory, synaptic plasticity and the ability of learning.[6]

Epidemiology

Around 100 cases have been described in medical literature.[7]

References
  1. Philadelphia, The Children's Hospital of (2020-05-19). "GRIN2B-Related Disorders". www.chop.edu. Archived from the original on 2021-12-14. Retrieved 2022-07-01.
  2. "GRIN2B related syndrome". NORD (National Organization for Rare Disorders). Archived from the original on 2022-05-13. Retrieved 2022-07-01.
  3. "GRIN2B-related neurodevelopmental disorder: MedlinePlus Genetics". medlineplus.gov. Archived from the original on 2021-10-23. Retrieved 2022-07-01.
  4. Platzer, Konrad; Lemke, Johannes R. (1993), Adam, Margaret P.; Mirzaa, Ghayda M.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "GRIN2B-Related Neurodevelopmental Disorder", GeneReviews®, Seattle (WA): University of Washington, Seattle, PMID 29851452, archived from the original on 2022-01-20, retrieved 2022-07-01
  5. "Pruebas genéticas - Alteración del desarrollo neurológico asociado con GRIN2B (GRIN2B-related neurodevelopmental disorder) – Gen GRIN2B. - IVAMI". www.ivami.com. Archived from the original on 2022-07-01. Retrieved 2022-07-01.
  6. "GRIN2B gene: MedlinePlus Genetics". medlineplus.gov. Archived from the original on 2021-04-22. Retrieved 2022-07-01.
  7. "GRIN2B-Related Neurodevelopmental Disorder". encyclopedia.pub. Archived from the original on 2022-07-01. Retrieved 2022-07-01.
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