Cerebro-costo-mandibular syndrome
Medical condition
Cerebro-costo-mandibular syndrome | |
---|---|
Specialty | Medical genetics |
Symptoms | Jaw, rib, and palate anomalies |
Usual onset | Birth |
Duration | Lifelong |
Causes | Genetic mutation |
Prevention | none |
Prognosis | Depends on the case |
Frequency | very rare, only 110 cases have been described in medical literature |
Deaths | - |
Cerebro-costo-mandibular syndrome is a very rare genetic disorder which is characterized by jaw/chin, palate and rib abnormalities.[1]
Signs and symptoms
The following list comprises the most common symptoms people with this disorder exhibit:[2]
- Severe micrognathia
- Thorax in the shape of a bell
- Cleft palate
- Neonatal respiratory difficulties
- Rib gaps
Common (but not the most) symptoms include:
- External auditory canal atresia
- Hearing loss
- Failure to thrive
- Glossoptosis
- Intellectual disabilities
- Fetal growth delays
- Kyphosis
- Short height
- Tracheomalacia
Not common but also not rare symptoms include:
- Fifth finger clinodactyly
- Cerebral calcification
- Hydranencephaly
- Meningocele
- Microcephaly
- Polycystic kidney dysplasia
- Myelomeningocele
- Porencephalic cyst
- Short, hard palate
- Spina bifida
- Ventricular septal defect
- Webbed neck
Causes
This disorder is caused by autosomal dominant mutations in the SNRPB gene, in chromosome 20.[3]
Epidemiology
Only 110 cases have been described in medical literature.[4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20]
References
- ^ RESERVADOS, INSERM US14-- TODOS LOS DERECHOS. "Orphanet: Síndrome cerebrocostomandibular". www.orpha.net (in Spanish). Retrieved 2022-06-12.
{{cite web}}
: CS1 maint: numeric names: authors list (link) - ^ "Cerebro-costo-mandibular syndrome - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2022-06-12.
- ^ Lynch DC, Revil T, Schwartzentruber J, Bhoj EJ, Innes AM, Lamont RE, et al. (July 2014). "Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro-costo-mandibular syndrome". Nature Communications. 5 (1): 4483. Bibcode:2014NatCo...5.4483.. doi:10.1038/ncomms5483. PMC 4109005. PMID 25047197.
- ^ "OMIM Entry - # 117650 - CEREBROCOSTOMANDIBULAR SYNDROME; CCMS". omim.org. Retrieved 2022-06-12.
- ^ McNicholl B, Egan-Mitchell B, Murray JP, Doyle JF, Kennedy JD, Crome L (June 1970). "Cerebro-costo-mandibular syndrome. A new familial developmental disorder". Archives of Disease in Childhood. 45 (241): 421–424. doi:10.1136/adc.45.241.421. PMC 1647602. PMID 5427859.
- ^ Silverman FN, Strefling AM, Stevenson DK, Lazarus J (September 1980). "Cerebro-costo-mandibular syndrome". The Journal of Pediatrics. 97 (3): 406–416. doi:10.1016/s0022-3476(80)80190-9. PMID 7411303.
- ^ Leroy JG, Devos EA, Vanden Bulcke LJ, Robbe NS (September 1981). "Cerebro-costo-mandibular syndrome with autosomal dominant inheritance". The Journal of Pediatrics. 99 (3): 441–443. doi:10.1016/s0022-3476(81)80343-5. PMID 7264806.
- ^ "OMIM Entry - # 117650 - CEREBROCOSTOMANDIBULAR SYNDROME; CCMS". omim.org. Retrieved 2022-06-12.
- ^ Hennekam RC, Beemer FA, Huijbers WA, Hustinx PA, van Sprang FJ (August 1985). "The cerebro-costo-mandibular syndrome: third report of familial occurrence". Clinical Genetics. 28 (2): 118–121. doi:10.1111/j.1399-0004.1985.tb00370.x. PMID 3899422. S2CID 46433302.
- ^ Trautman MS, Schelley SL, Stevenson DK (December 1985). "Cerebro-costo-mandibular syndrome: a familial case consistent with autosomal recessive inheritance". The Journal of Pediatrics. 107 (6): 990–991. doi:10.1016/s0022-3476(85)80219-5. PMID 4067764.
- ^ Drossou-Agakidou V, Andreou A, Soubassi-Griva V, Pandouraki M (October 1991). "Cerebrocostomandibular syndrome in four sibs, two pairs of twins". Journal of Medical Genetics. 28 (10): 704–707. doi:10.1136/jmg.28.10.704. PMC 1017059. PMID 1941967.
- ^ Plötz FB, van Essen AJ, Bosschaart AN, Bos AP (March 1996). "Cerebro-costo-mandibular syndrome". American Journal of Medical Genetics. 62 (3): 286–292. doi:10.1002/(SICI)1096-8628(19960329)62:3<286::AID-AJMG16>3.0.CO;2-G. PMID 8882789.
- ^ Merlob P, Schonfeld A, Grunebaum M, Mor N, Reisner SH (January 1987). "Autosomal dominant cerebro-costo-mandibular syndrome: ultrasonographic and clinical findings". American Journal of Medical Genetics. 26 (1): 195–202. doi:10.1002/ajmg.1320260129. PMID 3544846.
- ^ Hennekam RC, Goldschmeding R (January 1998). "Complete absence of rib ossification, micrognathia and ear anomalies: extreme expression of cerebro-costo-mandibular syndrome?". European Journal of Human Genetics. 6 (1): 71–74. doi:10.1038/sj.ejhg.5200154. PMID 9781016. S2CID 30627133.
- ^ Kirk EP, Arbuckle S, Ramm PL, Adès LC (May 1999). "Severe micrognathia, cleft palate, absent olfactory tract, and abnormal rib development: cerebro-costo-mandibular syndrome or a new syndrome?". American Journal of Medical Genetics. 84 (2): 120–124. doi:10.1002/(SICI)1096-8628(19990521)84:2<120::AID-AJMG7>3.0.CO;2-3. PMID 10323736.
- ^ James PA, Aftimos S (January 2003). "Familial cerebro-costo-mandibular syndrome: a case with unusual prenatal findings and review". Clinical Dysmorphology. 12 (1): 63–68. doi:10.1097/00019605-200301000-00012. PMID 12514369. S2CID 41024939.
- ^ Su PH, Chen JY, Chiang CL, Ng YY, Chen SJ (April 2010). "Exclusion of MYF5, GSC, RUNX2, and TCOF1 mutation in a case of cerebro-costo-mandibular syndrome". Clinical Dysmorphology. 19 (2): 51–55. doi:10.1097/MCD.0b013e328335c133. PMID 20177378. S2CID 21435401.
- ^ Lynch DC, Revil T, Schwartzentruber J, Bhoj EJ, Innes AM, Lamont RE, et al. (July 2014). "Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro-costo-mandibular syndrome". Nature Communications. 5: 4483. Bibcode:2014NatCo...5.4483.. doi:10.1038/ncomms5483. PMC 4109005. PMID 25047197.
- ^ Bacrot S, Doyard M, Huber C, Alibeu O, Feldhahn N, Lehalle D, et al. (February 2015). "Mutations in SNRPB, encoding components of the core splicing machinery, cause cerebro-costo-mandibular syndrome". Human Mutation. 36 (2): 187–190. doi:10.1002/humu.22729. PMID 25504470. S2CID 7059448.
- ^ Tooley M, Lynch D, Bernier F, Parboosingh J, Bhoj E, Zackai E, et al. (May 2016). "Cerebro-costo-mandibular syndrome: Clinical, radiological, and genetic findings". American Journal of Medical Genetics. Part A. 170A (5): 1115–1126. doi:10.1002/ajmg.a.37587. PMID 26971886. S2CID 26104190.