Literature DB >> 1920368

Single maxillary central incisor in a girl with del(18p) syndrome.

D J Aughton1, A A AlSaadi, D J Transue.   

Abstract

We present a girl with del(18p) syndrome and a single maxillary central incisor; she is only the second patient in whom this association has been reported.

Entities:  

Mesh：

Year:  1991        PMID： 1920368      PMCID： PMC1016981          DOI： 10.1136/jmg.28.8.530

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  2 in total

Review 1.  Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities.

Authors:  M M Cohen
Journal:  Am J Med Genet       Date:  1989-10

2.  18p - syndrome with a single central maxillary incisor.

Authors:  L M Dolan; K Willson; W G Wilson
Journal:  J Med Genet       Date:  1981-10       Impact factor: 6.318
  2 in total
  11 in total

1.  Minimal evidence for a direct involvement of twisted gastrulation homolog 1 (TWSG1) gene in human holoprosencephaly.

Authors:  Emily F Kauvar; Ping Hu; Daniel E Pineda-Alvarez; Benjamin D Solomon; Amalia Dutra; Evgenia Pak; Brooke Blessing; Virginia Proud; Alan L Shanske; Cathy A Stevens; Jill A Rosenfeld; Lisa G Shaffer; Erich Roessler; Maximilian Muenke
Journal:  Mol Genet Metab       Date:  2010-12-21       Impact factor: 4.797

2.  Del(18p) syndrome with a single central maxillary incisor.

Authors:  E Morales Peralta; A Lantigua
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318

3.  TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype.

Authors:  A A Keaton; B D Solomon; E F Kauvar; K B El-Jaick; A L Gropman; Y Zafer; J M Meck; S J Bale; D K Grange; B R Haddad; G C Gowans; N J Clegg; M R Delgado; J S Hahn; D E Pineda-Alvarez; F Lacbawan; J I Vélez; E Roessler; M Muenke
Journal:  Mol Syndromol       Date:  2011-05-18

4.  Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.

Authors:  S W Horsley; S J Knight; J Nixon; S Huson; M Fitchett; R A Boone; D Hilton-Jones; J Flint; L Kearney
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

5.  Solitary Median Maxillary Central Incisor due to Nasal Pyriform Aperture Stenosis in Fetus: The First Prenatal Ultrasound Case Report.

Authors:  Florent Fuchs; Manon Chadelle; Guillaume Captier; Olivier Prodhomme; Jean Michel Faure
Journal:  Int J Clin Pediatr Dent       Date:  2020 May-Jun

Review 6.  Solitary median maxillary central incisor syndrome (SMMCI) with congenital nasal puriform aperture stenosis: literature review and case report with comprehensive dental treatment and 14 years follow-up.

Authors:  N N Lygidakis; K Chatzidimitriou; N Petrou; N A Lygidakis
Journal:  Eur Arch Paediatr Dent       Date:  2013-06-18

7.  Physical mapping of the holoprosencephaly critical region in 18p11.3.

Authors:  J Overhauser; H F Mitchell; E H Zackai; D B Tick; K Rojas; M Muenke
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

8.  Solitary median maxillary central incisor in association with hemifacial microsomia: A rare case report and review of literature.

Authors:  Ashok Utreja; Syed Naved Zahid; Richa Gupta
Journal:  Contemp Clin Dent       Date:  2011-10

Review 9.  Solitary median maxillary central incisor (SMMCI) syndrome.

Authors:  Roger K Hall
Journal:  Orphanet J Rare Dis       Date:  2006-04-09       Impact factor: 4.123

10.  Solitary median maxillary central incisor syndrome: A rare entity.

Authors:  Anurag Negi; Amita Negi; Megha Mohanan
Journal:  J Oral Maxillofac Pathol       Date:  2020-09-09
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