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Quoted phrase not found in phrase index: "Single Central Incisor Syndrome"
Page 1
The solitary median maxillary central incisor (SMMCI) syndrome: Associations, prenatal diagnosis, and outcomes.
Garcia Rodriguez R, Garcia Cruz L, Novoa Medina Y, Garcia Delgado R, Perez Gonzalez J, Palma Milla C, Lopez Siles J, Medina Castellano M, Garcia Hernandez JA, Santana Rodriguez A. Garcia Rodriguez R, et al. Prenat Diagn. 2019 May;39(6):415-419. doi: 10.1002/pd.5451. Epub 2019 Apr 26. Prenat Diagn. 2019. PMID: 30900264 Review.
Solitary median maxillary central incisor (SMMCI) syndrome is a complex disorder consisting of multiple, developmental defects involving midline structures of the head, which includes the cranial bones, the maxilla, and its container dentition (specifically t …
Solitary median maxillary central incisor (SMMCI) syndrome is a complex disorder consisting of multiple, developmental …
The primary Maxillary Central Incisor in the Solitary Median Maxillary Central Incisor syndrome.
Kjaer I, Balslev-Olesen M. Kjaer I, et al. Eur J Paediatr Dent. 2012 Mar;13(1):73-5. Eur J Paediatr Dent. 2012. PMID: 22455533
AIM: Solitary Median Maxillary Central Incisor (SMMCI) is a developmental anomaly in the permanent dentition with one single central incisor in the maxilla, positioned exactly in the midline. ...The aim was to analyse whether a permanent sing …
AIM: Solitary Median Maxillary Central Incisor (SMMCI) is a developmental anomaly in the permanent dentition with one singl …
Selected clinical research involving the central nervous system.
Cohen MM Jr. Cohen MM Jr. J Craniofac Genet Dev Biol. 1990;10(2):215-38. J Craniofac Genet Dev Biol. 1990. PMID: 2211967 Review.
The relationship between oculo-auriculo-vetebral spectrum with encephalocele and frontonasal dysplasia with epibulbar dermoids and ear tags is also discussed and an explanation for encephalocele formation in the Apert syndrome is provided. Studies of the central ner …
The relationship between oculo-auriculo-vetebral spectrum with encephalocele and frontonasal dysplasia with epibulbar dermoids and ear tags …
KBG syndrome: Common and uncommon clinical features based on 31 new patients.
Gnazzo M, Lepri FR, Dentici ML, Capolino R, Pisaneschi E, Agolini E, Rinelli M, Alesi V, Versacci P, Genovese S, Cesario C, Sinibaldi L, Baban A, Bartuli A, Marino B, Cappa M, Dallapiccola B, Novelli A, Digilio MC. Gnazzo M, et al. Am J Med Genet A. 2020 May;182(5):1073-1083. doi: 10.1002/ajmg.a.61524. Epub 2020 Mar 3. Am J Med Genet A. 2020. PMID: 32124548
KBG syndrome (MIM #148050) is an autosomal dominant disorder characterized by developmental delay, intellectual disability, distinct craniofacial anomalies, macrodontia of permanent upper central incisors, skeletal abnormalities, and short stature. ...It is l …
KBG syndrome (MIM #148050) is an autosomal dominant disorder characterized by developmental delay, intellectual disability, distinct …
Single median maxillary central incisor syndrome and variant in SMO gene associated with SHH pathway.
Zatoński T, Pazdro-Zastawny K, Morawska-Kochman M, Biela M, Kołtowska A, Rydzanicz M, Rozensztrauch A, Kosińska J, Dorobisz K, Płoski R, Śmigiel R. Zatoński T, et al. Int J Pediatr Otorhinolaryngol. 2020 Jul;134:110038. doi: 10.1016/j.ijporl.2020.110038. Epub 2020 Apr 13. Int J Pediatr Otorhinolaryngol. 2020. PMID: 32335464
Solitary median maxillary central incisor syndrome (SMMCI) is a rare congenital oronasal-dental midline anomaly. ...
Solitary median maxillary central incisor syndrome (SMMCI) is a rare congenital oronasal-dental midline anomaly. ...
KBG syndrome in a Chinese population: A case series.
Ho S, Luk HM, Lo IFM. Ho S, et al. Am J Med Genet A. 2022 Jun;188(6):1693-1699. doi: 10.1002/ajmg.a.62688. Epub 2022 Feb 17. Am J Med Genet A. 2022. PMID: 35174959
KBG syndrome (OMIM #148050) is an autosomal dominant neurodevelopmental disorder characterized by the presence of macrodontia of the permanent central upper incisors, characteristic facial features, delay in development, intellectual disability, short stature …
KBG syndrome (OMIM #148050) is an autosomal dominant neurodevelopmental disorder characterized by the presence of macrodontia of the …
Williams syndrome--oral presentation of 45 cases.
Hertzberg J, Nakisbendi L, Needleman HL, Pober B. Hertzberg J, et al. Pediatr Dent. 1994 Jul-Aug;16(4):262-7. Pediatr Dent. 1994. PMID: 7937257 Review.
Forty-five patients with Williams syndrome (WS) were evaluated for oral abnormalities. The mean age of the patients was 9.25 years, the median age was 6.7 years, and the majority (62.2%) were male. ...Abnormal tooth morphology was noted in 12.5% of the primary dentitions a …
Forty-five patients with Williams syndrome (WS) were evaluated for oral abnormalities. The mean age of the patients was 9.25 years, t …
Solitary median maxillary central incisor syndrome and holoprosencephaly: a case report.
Viana Eda S, Kramer PF, Closs LQ, Scalco G. Viana Eda S, et al. Pediatr Dent. 2010 Sep-Oct;32(5):424-7. Pediatr Dent. 2010. PMID: 21070710
Solitary median maxillary central incisor syndrome (SMMCIS) is a rare anomaly that affects 1 in 50,000 live births. ...The purposes of this paper were to: describe the clinical case of an 8-year-old boy with a permanent central incisor located a …
Solitary median maxillary central incisor syndrome (SMMCIS) is a rare anomaly that affects 1 in 50,000 live births. ... …
Surgical management of multiple supernumerary teeth and an impacted maxillary permanent central incisor.
Rallan M, Rallan NS, Goswami M, Rawat K. Rallan M, et al. BMJ Case Rep. 2013 May 22;2013:bcr2013009995. doi: 10.1136/bcr-2013-009995. BMJ Case Rep. 2013. PMID: 23704467 Free PMC article.
A case of 13 year male patient is reported with a multiple impacted supernumerary tooth in maxillary anterior region hindering the eruption of right permanent central incisor. The supernumerary tooth was treated via surgical approach followed by an interim prosthesi …
A case of 13 year male patient is reported with a multiple impacted supernumerary tooth in maxillary anterior region hindering the eruption …
The first case report of Stromme syndrome in a Chinese patient: Expanding the phenotype and literature review.
Ho S, Luk HM, Lo IFM. Ho S, et al. Am J Med Genet A. 2022 May;188(5):1626-1629. doi: 10.1002/ajmg.a.62646. Epub 2022 Jan 9. Am J Med Genet A. 2022. PMID: 35001526 Review.
Stromme syndrome (MIM #243605) is a rare autosomal recessive ciliopathy resulting from compound heterozygous or homozygous pathogenic alterations in the CENPF gene (# 600236). ...(Arg3094*). He presented with microcephaly, unilateral microphthalmia, single centra …
Stromme syndrome (MIM #243605) is a rare autosomal recessive ciliopathy resulting from compound heterozygous or homozygous pathogenic …
19 results