| Literature DB >> 26971886 |
Madeleine Tooley1, Danielle Lynch2, Francois Bernier2, Jillian Parboosingh2, Elizabeth Bhoj3, Elaine Zackai3, Alistair Calder4, Nobue Itasaki5, Emma Wakeling6, Richard Scott7, Melissa Lees7, Jill Clayton-Smith8, Moira Blyth9, Jenny Morton10, Debbie Shears11, Usha Kini11, Tessa Homfray12, Angus Clarke13, Angela Barnicoat7, Colin Wallis14, Rebecca Hewitson14, Amaka Offiah15, Michael Saunders16, Simon Langton-Hewer17, Tom Hilliard17, Peter Davis18, Sarah Smithson1.
Abstract
Cerebro-Costo-Mandibular syndrome (CCMS) is a rare autosomal dominant condition comprising branchial arch-derivative malformations with striking rib-gaps. Affected patients often have respiratory difficulties, associated with upper airway obstruction, reduced thoracic capacity, and scoliosis. We describe a series of 12 sporadic and 4 familial patients including 13 infants/children and 3 adults. Severe micrognathia and reduced numbers of ribs with gaps are consistent findings. Cleft palate, feeding difficulties, respiratory distress, tracheostomy requirement, and scoliosis are common. Additional malformations such as horseshoe kidney, hypospadias, and septal heart defect may occur. Microcephaly and significant developmental delay are present in a small minority of patients. Key radiological findings are of a narrow thorax, multiple posterior rib gaps and abnormal costo-transverse articulation. A novel finding in 2 patients is bilateral accessory ossicles arising from the hyoid bone. Recently, specific mutations in SNRPB, which encodes components of the major spliceosome, have been found to cause CCMS. These mutations cluster in an alternatively spliced regulatory exon and result in altered SNRPB expression. DNA was available from 14 patients and SNRPB mutations were identified in 12 (4 previously reported). Eleven had recurrent mutations previously described in patients with CCMS and one had a novel mutation in the alternative exon. These results confirm the specificity of SNRPB mutations in CCMS and provide further evidence for the role of spliceosomal proteins in craniofacial and thoracic development.Entities:
Keywords: CCM syndrome; Cerebro-costo-mandibular syndrome; Pierre Robin syndrome; micrognathia; rib gaps
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Year: 2016 PMID: 26971886 DOI: 10.1002/ajmg.a.37587
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802