Cleft lip and/or palate in two cases of 46,X,i(Xq) Turner syndrome

Genetic Counseling

Volumn 13, Issue 1, 2002, Pages 19-22

  Corona Rivera, J R ^a   Corona Rivera, E ^a   Bobadilla Morales, L ^a   Garcia Cobian, T A ^a   Corona Rivera, A ^a  

^a Laboratorio de Genetica Humana   (Mexico)

Author keywords

Bifid uvula; Cleft lip; Cleft palate; Isochromosome Xq; Turner syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME XQ; CLEFT LIP; CLEFT LIP PALATE; CLEFT PALATE; DERMATOGLYPHICS; FACE MALFORMATION; FEMALE; GENE DOSAGE; HUMAN; HUMAN CELL; ISOCHROMOSOME X; KARYOTYPE 46,XX; KLINEFELTER SYNDROME; SUPERNUMERARY CHROMOSOME; TURNER SYNDROME; X CHROMOSOME;

CHILD; CHILD, PRESCHOOL; CLEFT LIP; CLEFT PALATE; FEMALE; HUMANS; ISOCHROMOSOMES; TURNER SYNDROME; UVULA;

EID: 0036209985     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (14)

1. Clinical and cytogenetic findings in 74 patients with Turner's syndrome seen in a pediatric hospital
2. Morphological characteristics of monosomy X in spontaneous abortions
3. Abordaje semiológico de tres diferentes constituciones cromosómicas en el síndrome de Turner. Parte II. Fenotipo clínico
4. Trisomy Xq in male: The isochromosome X Klinefelter syndrome
5. Oral and dental development in X chromosome aneuploidy
6. Pentasomy X: Report of patient and studies of X-inactivation
7. Facial clefting and its syndromes
8. The epidemiology of orofacial clefts. 2. Associated malformations
9. Turner syndrome: II. Associated anomalies, mental performance and psychological problems in 218 patients diagnosed in Leuven in the period 1965-1989
10. Familial occurrence of isodicentric X chromosomes with different breakpoints
11. Turner syndrome and female sex chromosome aberrations: Deduction of the principal factors involved in the development of clinical features
12. The Turner phenotype and the different types of human X isochromosome
13. Dermatoglyphic differences between 45,X and other chromosomal abnormalities of Turner syndrome
14. Summary of clinical findings: Profiles of children with 47,XXY, 47,XXX and 47,XYY karyotypes