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Year Number of Results
1998 2
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2002 1
2003 5
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2006 4
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2008 2
2009 10
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2011 12
2012 9
2013 3
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133 results

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Page 1
Muenke syndrome.
Sabatino G, Di Rocco F, Zampino G, Tamburrini G, Caldarelli M, Di Rocco C. Sabatino G, et al. Childs Nerv Syst. 2004 May;20(5):297-301. doi: 10.1007/s00381-003-0906-y. Epub 2004 Feb 10. Childs Nerv Syst. 2004. PMID: 14963686
BACKGROUND: Muenke syndrome is a genetically determined craniosynostosis that involves one or both coronal sutures. ...ILLUSTRATIVE CASES: We report the cases of two sisters who presented with Muenke syndrome and whose affected mother did not ha …
BACKGROUND: Muenke syndrome is a genetically determined craniosynostosis that involves one or both coronal sutures. ... …
Craniosynostosis: Current Evaluation and Management.
Sullivan LE, Li R, Tong VS, Jagasia P, Bonfield CM, Golinko MS, Pontell ME. Sullivan LE, et al. Ann Plast Surg. 2024 Dec 1;93(6S Suppl 3):S144-S149. doi: 10.1097/SAP.0000000000004131. Ann Plast Surg. 2024. PMID: 39527402 Review.
Craniosynostosis is characterized by the premature fusion of one or more cranial sutures, which can lead to abnormal skull shape and restricted skull growth. Although most cases are present in isolation, some are associated with genetic syndromes, such as Pfeiffer, Muen …
Craniosynostosis is characterized by the premature fusion of one or more cranial sutures, which can lead to abnormal skull shape and …
Human Genetics of Ventricular Septal Defect.
Perrot A, Rickert-Sperling S. Perrot A, et al. Adv Exp Med Biol. 2024;1441:505-534. doi: 10.1007/978-3-031-44087-8_27. Adv Exp Med Biol. 2024. PMID: 38884729
Syndromic Craniosynostosis.
Sawh-Martinez R, Steinbacher DM. Sawh-Martinez R, et al. Clin Plast Surg. 2019 Apr;46(2):141-155. doi: 10.1016/j.cps.2018.11.009. Clin Plast Surg. 2019. PMID: 30851747 Review.
The most common craniosynostosis syndromes include Apert (FGFR2), Crouzon (FGFR2), Muenke (FGFR3), Pfeiffer (FGFR1 and FGFR2), and Saethre-Chotzen (TWIST). Bicoronal craniosynostosis (turribrachycephaly) is most commonly associated with syndromic craniosyn …
The most common craniosynostosis syndromes include Apert (FGFR2), Crouzon (FGFR2), Muenke (FGFR3), Pfeiffer (FGFR1 and FGFR2), …
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.
Syndromic craniosynostosis affects up to 1:30,000 live births with characteristic craniofacial growth restrictions, deformities, and other associated abnormalities, such as carpal-pedal anomalies and cognitive function impairment. More than 150 syndromes are associated wit …
Syndromic craniosynostosis affects up to 1:30,000 live births with characteristic craniofacial growth restrictions, deformities, and …
Craniofacial syndromes.
Buchanan EP, Xue AS, Hollier LH Jr. Buchanan EP, et al. Plast Reconstr Surg. 2014 Jul;134(1):128e-153e. doi: 10.1097/PRS.0000000000000308. Plast Reconstr Surg. 2014. PMID: 25028828 Review.
Craniosynostosis is a congenital disorder in which one or more of the cranial sutures fuses prematurely. ...As with syndromes associated with craniosynostosis, the key to management is a multidisciplinary approach focused on the right timing. ...
Craniosynostosis is a congenital disorder in which one or more of the cranial sutures fuses prematurely. ...As with syndromes associa …
Syndromic Craniosynostosis: Unique Management Considerations.
Hersh DS, Hughes CD. Hersh DS, et al. Neurosurg Clin N Am. 2022 Jan;33(1):105-112. doi: 10.1016/j.nec.2021.09.008. Epub 2021 Oct 26. Neurosurg Clin N Am. 2022. PMID: 34801135 Review.
Craniosynostosis involves the premature fusion of 1 or more cranial sutures and commonly presents as an isolated, nonsyndromic diagnosis. A subset of patients have syndromic craniosynostosis. Several unique considerations must be taken into account when managing pat …
Craniosynostosis involves the premature fusion of 1 or more cranial sutures and commonly presents as an isolated, nonsyndromic diagno …
Craniosynostosis: Neonatal Perspectives.
Bautista G. Bautista G. Neoreviews. 2021 Apr;22(4):e250-e257. doi: 10.1542/neo.22-4-e250. Neoreviews. 2021. PMID: 33795400
Primary or congenital craniosynostoses represent the majority of cases and consist of single-suture and multisuture synostoses. Multisuture synostoses are typically associated with distinct craniofacial syndromes, including Muenke syndrome, Apert syndrome, Cr …
Primary or congenital craniosynostoses represent the majority of cases and consist of single-suture and multisuture synostoses. Multi …
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.
The term "craniosynostosis" was combined with the following key-words: ENT, apneas, OSAS, sleep-disordered breathing, tonsillectomy, deafness, hearing loss. ...Its main cause is otitis media with effusion (OME) but ossicular malformations and sensorineural hearing loss (SN …
The term "craniosynostosis" was combined with the following key-words: ENT, apneas, OSAS, sleep-disordered breathing, tonsillectomy, …
Craniofacial morphology and growth in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis.
Choi TM, Lijten OW, Mathijssen IMJ, Wolvius EB, Ongkosuwito EM. Choi TM, et al. Clin Oral Investig. 2022 Mar;26(3):2927-2936. doi: 10.1007/s00784-021-04275-y. Epub 2021 Dec 14. Clin Oral Investig. 2022. PMID: 34904178 Free PMC article.
OBJECTIVES: To determine whether the midface of patients with Muenke syndrome, Saethre-Chotzen syndrome, or TCF12-related craniosynostosis is hypoplastic compared to skeletal facial proportions of a Dutch control group. ...CONCLUSIONS: In this study, we showe …
OBJECTIVES: To determine whether the midface of patients with Muenke syndrome, Saethre-Chotzen syndrome, or TCF12-related c …
133 results