BACKGROUND: Nicolaides-Baraitser and Coffin-Siris syndromes are emerging conditions with overlapping clinical features including intellectual disability and typical somatic characteristics, especially sparse hair, low frontal hairline, large mouth with thick and everted lips, and hands and feet anomalies. Since 2012, mutations in genes encoding six proteins of the BAF complex were identified in both conditions. METHODS AND RESULTS: We have clinically evaluated a cohort of 1161 patients with intellectual disability from three different Italian centers. A strong clinical suspicion of either Nicolaides-Baraitser syndrome or Coffin-Siris syndrome was proposed in 11 cases who were then molecularly confirmed: 8 having de novo missense mutations in SMARCA2, two frame-shift mutations in ARID1B and one missense mutation in SMARCB1. Given the high frequency of the condition we set up a one-step deep sequencing test for all 6 genes of the BAF complex. CONCLUSIONS: These results prove that the frequency of these conditions may be as high as the most common syndromes with intellectual deficit (about 1%). Clinical geneticists should be well aware of this group of disorders in the clinical setting when ascertaining patients with intellectual deficit, the specific facial features being the major diagnostic handle. Finally, this work adds information on the clinical differences of the two conditions and presents a fast and sensitive test for the molecular diagnosis. Copyright © 2014 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved

Mari, F., Marozza, A., Mencarelli, M.A., Lo Rizzo, C., Fallerini, C., Dosa, L., et al. (2015). Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability. BRAIN & DEVELOPMENT, 37(5), 527-536 [10.1016/j.braindev.2014.08.009].

Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability.

MARI, FRANCESCA;MENCARELLI, MARIA ANTONIETTA;Fallerini C;GROSSO, SALVATORE;RUBEGNI, PIETRO;CAFFARELLI, CARLA;PRETEGIANI, ELENA;FIMIANI, MICHELE;NUTI, RANUCCIO;DOTTI, MARIA;BALESTRI, PAOLO;RENIERI, ALESSANDRA
2015-01-01

Abstract

BACKGROUND: Nicolaides-Baraitser and Coffin-Siris syndromes are emerging conditions with overlapping clinical features including intellectual disability and typical somatic characteristics, especially sparse hair, low frontal hairline, large mouth with thick and everted lips, and hands and feet anomalies. Since 2012, mutations in genes encoding six proteins of the BAF complex were identified in both conditions. METHODS AND RESULTS: We have clinically evaluated a cohort of 1161 patients with intellectual disability from three different Italian centers. A strong clinical suspicion of either Nicolaides-Baraitser syndrome or Coffin-Siris syndrome was proposed in 11 cases who were then molecularly confirmed: 8 having de novo missense mutations in SMARCA2, two frame-shift mutations in ARID1B and one missense mutation in SMARCB1. Given the high frequency of the condition we set up a one-step deep sequencing test for all 6 genes of the BAF complex. CONCLUSIONS: These results prove that the frequency of these conditions may be as high as the most common syndromes with intellectual deficit (about 1%). Clinical geneticists should be well aware of this group of disorders in the clinical setting when ascertaining patients with intellectual deficit, the specific facial features being the major diagnostic handle. Finally, this work adds information on the clinical differences of the two conditions and presents a fast and sensitive test for the molecular diagnosis. Copyright © 2014 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved
Mari, F., Marozza, A., Mencarelli, M.A., Lo Rizzo, C., Fallerini, C., Dosa, L., et al. (2015). Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability. BRAIN & DEVELOPMENT, 37(5), 527-536 [10.1016/j.braindev.2014.08.009].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/905843