Literature DB >> 26971886

Cerebro-costo-mandibular syndrome: Clinical, radiological, and genetic findings.

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.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  CCM syndrome; Cerebro-costo-mandibular syndrome; Pierre Robin syndrome; micrognathia; rib gaps

Mesh:

Substances:

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


  7 in total

1.  Snrpb is required in murine neural crest cells for proper splicing and craniofacial morphogenesis.

Authors:  Sabrina Shameen Alam; Shruti Kumar; Marie-Claude Beauchamp; Eric Bareke; Alexia Boucher; Nadine Nzirorera; Yanchen Dong; Reinnier Padilla; Si Jing Zhang; Jacek Majewski; Loydie A Jerome-Majewska
Journal:  Dis Model Mech       Date:  2022-06-23       Impact factor: 5.732

2.  Clinical application of chromosomal microarray analysis for fetuses with craniofacial malformations.

Authors:  Chenyang Xu; Yanbao Xiang; Xueqin Xu; Lili Zhou; Huanzheng Li; Xueqin Dong; Shaohua Tang
Journal:  Mol Cytogenet       Date:  2020-08-25       Impact factor: 2.009

Review 3.  Developmental processes regulate craniofacial variation in disease and evolution.

Authors:  Fjodor Merkuri; Jennifer L Fish
Journal:  Genesis       Date:  2018-10-01       Impact factor: 2.487

4.  Local modulation of the Wnt/β-catenin and bone morphogenic protein (BMP) pathways recapitulates rib defects analogous to cerebro-costo-mandibular syndrome.

Authors:  Benedict R H Turner; Nobue Itasaki
Journal:  J Anat       Date:  2019-12-29       Impact factor: 2.610

5.  Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.

Authors:  Ella M M A Martin; Annabelle Enriquez; Duncan B Sparrow; David T Humphreys; Aideen M McInerney-Leo; Paul J Leo; Emma L Duncan; Kavitha R Iyer; Joelene A Greasby; Eddie Ip; Eleni Giannoulatou; Delicia Sheng; Elizabeth Wohler; Clémantine Dimartino; Jeanne Amiel; Yline Capri; Daphné Lehalle; Adi Mory; Yael Wilnai; Yael Lebenthal; Ali G Gharavi; Grażyna G Krzemień; Monika Miklaszewska; Robert D Steiner; Cathy Raggio; Robert Blank; Hagit Baris Feldman; Hila Milo Rasouly; Nara L M Sobreira; Rebekah Jobling; Christopher T Gordon; Philip F Giampietro; Sally L Dunwoodie; Gavin Chapman
Journal:  Hum Mol Genet       Date:  2020-12-04       Impact factor: 6.150

6.  PUF60 variants cause a syndrome of ID, short stature, microcephaly, coloboma, craniofacial, cardiac, renal and spinal features.

Authors:  Karen J Low; Morad Ansari; Rami Abou Jamra; Angus Clarke; Salima El Chehadeh; David R FitzPatrick; Mark Greenslade; Alex Henderson; Jane Hurst; Kory Keller; Paul Kuentz; Trine Prescott; Franziska Roessler; Kaja K Selmer; Michael C Schneider; Fiona Stewart; Katrina Tatton-Brown; Julien Thevenon; Magnus D Vigeland; Julie Vogt; Marjolaine Willems; Jonathan Zonana; D D D Study; Sarah F Smithson
Journal:  Eur J Hum Genet       Date:  2017-03-22       Impact factor: 4.246

Review 7.  Emerging roles of spliceosome in cancer and immunity.

Authors:  Hui Yang; Bruce Beutler; Duanwu Zhang
Journal:  Protein Cell       Date:  2021-07-01       Impact factor: 15.328

  7 in total

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