Nicolaides–Baraitser syndrome
Medical condition
Nicolaides–Baraitser syndrome
Nicolaides–Baraitser syndrome (NCBRS) is a rare genetic condition caused by de novo missense mutations in the SMARCA2 gene and has only been reported in fewer than 330 cases worldwide. NCBRS is a distinct condition and well recognizable once the symptoms have been identified. Another condition associated with changes in the SMARCA2 gene is Coffin–Siris syndrome.
Read on Wikipedia · Image Chater-Diehl, E., Ejaz, R., Cytrynbaum, C. et al., CC BY 4.0
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