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Page 1
Assessing the midface in Muenke syndrome: A cephalometric analysis and review of the literature.
Samra F, Bauder AR, Swanson JW, Whitaker LA, Bartlett SP, Taylor JA. Samra F, et al. J Plast Reconstr Aesthet Surg. 2016 Sep;69(9):1285-90. doi: 10.1016/j.bjps.2016.06.017. Epub 2016 Jul 16. J Plast Reconstr Aesthet Surg. 2016. PMID: 27449747 Review.
METHODS: We retrospectively reviewed all patients with a genetic and clinical diagnosis of Muenke syndrome from 1990 to 2014. Review of clinical records and photographs included skeletal Angle Class, dental occlusion, and incidence of orthognathic intervention. ...O …
METHODS: We retrospectively reviewed all patients with a genetic and clinical diagnosis of Muenke syndrome from 1990 to 2014. …
Syndromic Craniosynostosis.
Wang JC, Nagy L, Demke JC. Wang JC, et al. Facial Plast Surg Clin North Am. 2016 Nov;24(4):531-543. doi: 10.1016/j.fsc.2016.06.008. Facial Plast Surg Clin North Am. 2016. PMID: 27712819 Review.
Palatal and oral manifestations of Muenke syndrome (FGFR3-related craniosynostosis).
Agochukwu NB, Solomon BD, Doherty ES, Muenke M. Agochukwu NB, et al. J Craniofac Surg. 2012 May;23(3):664-8. doi: 10.1097/SCS.0b013e31824db8bb. J Craniofac Surg. 2012. PMID: 22565872 Free PMC article. Review.
Although Muenke syndrome is the most common syndromic form of craniosynostosis, the frequency of oral and palatal anomalies including high-arched palate, cleft lip with or without cleft palate has not been documented in a patient series of Muenke syndrome …
Although Muenke syndrome is the most common syndromic form of craniosynostosis, the frequency of oral and palatal anomalies in …
Craniosynostosis and ENT.
Couloigner V, Ayari Khalfallah S. Couloigner V, et al. Neurochirurgie. 2019 Nov;65(5):318-321. doi: 10.1016/j.neuchi.2019.09.015. Epub 2019 Sep 27. Neurochirurgie. 2019. PMID: 31568777 Review.
Its main cause is otitis media with effusion (OME) but ossicular malformations and sensorineural hearing loss (SNHL) are sometimes observed. SNHL is mostly found in Muenke syndrome. In view of the frequency and potential severity of these disorders into account, yea …
Its main cause is otitis media with effusion (OME) but ossicular malformations and sensorineural hearing loss (SNHL) are sometimes observed. …
Talocalcaneal coalition in Muenke syndrome: report of a patient, review of the literature in FGFR-related craniosynostoses, and consideration of mechanism.
Agochukwu NB, Solomon BD, Benson LJ, Muenke M. Agochukwu NB, et al. Am J Med Genet A. 2013 Mar;161A(3):453-60. doi: 10.1002/ajmg.a.35233. Epub 2013 Feb 1. Am J Med Genet A. 2013. PMID: 23378035 Free PMC article. Review.
Tarsal coalition is a distinct feature of Muenke syndrome and has been reported since the initial description of the disorder in the 1990s. Although talocalcaneal coalition is the most common tarsal coalition in the general population, it has never previously been r …
Tarsal coalition is a distinct feature of Muenke syndrome and has been reported since the initial description of the disorder …
A familial case of Muenke syndrome. Diverse expressivity of the FGFR3 Pro252Arg mutation--case report and review of the literature.
Aravidis C, Konialis CP, Pangalos CG, Kosmaidou Z. Aravidis C, et al. J Matern Fetal Neonatal Med. 2014 Sep;27(14):1502-6. doi: 10.3109/14767058.2013.860520. Epub 2013 Nov 29. J Matern Fetal Neonatal Med. 2014. PMID: 24168007 Review.
Muenke is a fibroblast growth factor receptor 3 (FGFR-3)-associated syndrome, which was first described in late 1990 s. Muenke syndrome is an autosomal dominant disorder characterized mainly by coronal suture craniosynostosis, hearing impairment and intellectual dis …
Muenke is a fibroblast growth factor receptor 3 (FGFR-3)-associated syndrome, which was first described in late 1990 s. Muenke syn …
Epilepsy in Muenke syndrome: FGFR3-related craniosynostosis.
Agochukwu NB, Solomon BD, Gropman AL, Muenke M. Agochukwu NB, et al. Pediatr Neurol. 2012 Nov;47(5):355-61. doi: 10.1016/j.pediatrneurol.2012.07.004. Pediatr Neurol. 2012. PMID: 23044018 Free PMC article. Review.
We present seven patients with Muenke syndrome and seizures. A review of 789 published cases of Muenke syndrome, with a focus on epilepsy and intracranial anomalies in Muenke syndrome, revealed epilepsy in six patients, with intracranial …
We present seven patients with Muenke syndrome and seizures. A review of 789 published cases of Muenke syndrome, …
Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings.
Agochukwu NB, Solomon BD, Muenke M. Agochukwu NB, et al. Int J Pediatr Otorhinolaryngol. 2014 Dec;78(12):2037-47. doi: 10.1016/j.ijporl.2014.09.019. Epub 2014 Sep 28. Int J Pediatr Otorhinolaryngol. 2014. PMID: 25441602 Review.
OBJECTIVE: This review addresses hearing loss as it occurs and has been reported in Muenke syndrome as well as six additional FGFR related craniosynostosis syndromes (Apert syndrome, Pfeiffer syndrome, Crouzon syndrome, Beare-Stevenson syndrome, Crouzon syndrome wit …
OBJECTIVE: This review addresses hearing loss as it occurs and has been reported in Muenke syndrome as well as six additional …
Imaging of Skeletal Disorders Caused by Fibroblast Growth Factor Receptor Gene Mutations.
Sargar KM, Singh AK, Kao SC. Sargar KM, et al. Radiographics. 2017 Oct;37(6):1813-1830. doi: 10.1148/rg.2017170017. Radiographics. 2017. PMID: 29019756 Review.
Disorders caused by type 3 mutations include achondroplasia, hypochondroplasia, thanatophoric dysplasia (TD), severe achondroplasia with developmental delay and acanthosis nigricans, Crouzonodermoskeletal syndrome, and Muenke syndrome. Most of these mutations are in …
Disorders caused by type 3 mutations include achondroplasia, hypochondroplasia, thanatophoric dysplasia (TD), severe achondroplasia with dev …
Hearing loss in syndromic craniosynostoses: introduction and consideration of mechanisms.
Agochukwu NB, Solomon BD, Muenke M. Agochukwu NB, et al. Am J Audiol. 2014 Jun;23(2):135-41. doi: 10.1044/2014_AJA-13-0036. Am J Audiol. 2014. PMID: 24686979 Free PMC article. Review.
CONCLUSION: The variable auditory phenotypes seen in individuals with Muenke syndrome may have a genetic basis, likely due to multiple interacting factors in the genetic environment or modifying factors. Further analysis and studies of mouse models of Muenke …
CONCLUSION: The variable auditory phenotypes seen in individuals with Muenke syndrome may have a genetic basis, likely due to …
11 results