Full text in pdf format

 

Deletion 18p associated with a single maxillary incisor: a case study

 

 

Estela Morales-Peralta; Aracely Lantigua

Centro Nacional de Genética Médica, Escuela de Medicina Victoria de Girón, 146 # 3102, Playa, Ciudad de la Habana, Cuba. Send correspondence to E.M.-P.

 

 


ABSTRACT

We describe a patient with del(18p) syndrome and with a single central maxillary incisor (SCMI). There are few reports on this association. SCMI could be a less severe form of holoprosencephaly in del(18p) syndrome.

Keywords: deletion 18p; single maxillary; incisor.


 

 

REFERENCES

Aughton, D.J., Alsaadi, A.A. and Transue, D.J. (1991). Single maxillary central incisor in a girl with del(18p) syndrome. J. Med. Genet. 28: 530-532.

Berry, S.A., Pierpont, M.E. and Gorlin, R.J. (1984). Single central incisor in familial holoprosencephaly. J. Pediatr. 104: 877-880.

Boudailliez, B., Morichon-Delvallez, N., Goldfarb, A., Pautard, J.C.L., Lenaerts, C. and Piussan, C.H. (1983). Incisive supérieure unique, hypopituitarisme et anomalie chromosomique monosomie 18p. J. Génét. Hum. 31: 239-242.

Dolan, L.M., Willson, K. and Wilson, W.G. (1981). 18p Syndrome with a single central maxillary incisor. J. Med. Genet. 18: 396-398.

Masuno, M., Fukushima, Y., Sugio, Y., Ikeda, M. and Kuroki, Y. (1990). Two unrelated cases of single maxillary central incisor with 7q terminal deletion. Jpn. J. Human. Genet. 35: 311-317.

Schinzel, A. (1983). Catalogue of Unbalanced Chromosome Aberrations in Man. Walter de Gruyter, Berlin, pp. 604-668.