Sotos syndrome: Evolution of facial phenotype subjective and objective assessment

American Journal of Medical Genetics

Volumn 65, Issue 1, 1996, Pages 13-20

  Allanson, Judith E ^a   Cole, Trevor R P ^b  

^a CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^b Birmingham Research Unit   (United Kingdom)

Author keywords

anthropometry; craniofacial pattern profiles; facial phenotype; Sotos syndrome

Indexed keywords

ADOLESCENT; ADULT; ANTHROPOMETRY; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; CRANIOFACIAL MORPHOLOGY; FACE MALFORMATION; FEMALE; FOREHEAD; HEAD; HUMAN; INFANT; MALE; PHENOTYPE; PHOTOGRAPHY; PRIORITY JOURNAL; SOTOS SYNDROME;

ADOLESCENT; ADULT; AGING; ANTHROPOMETRY; CHILD; CHILD, PRESCHOOL; CRANIOFACIAL ABNORMALITIES; FACE; FEMALE; GIGANTISM; GROWTH DISORDERS; HUMANS; INFANT; MALE; PHENOTYPE; SYNDROME;

EID: 0029815064     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19961002)65:1<13::AID-AJMG2>3.0.CO;2-Z     Document Type: Article

References (21)

1. Allanson JE, Hall JG, Hughes HE, Preus M, Witt D (1985): Noonan syndrome: An evolving phenotype. Am J Med Genet 21:507-514.
2. Allanson JE (1988): G syndrome: An unusual family. Am J Med Genet 31:637-642.
3. Allanson JE (1989): Time and natural history: The changing face. J Craniofac Genet Devel Biol 9:21-28.
4. Allanson JE (1990): Rubinstein-Taybi syndrome: The changing face. Am J Med Genet Suppl 6:38-41.
5. Allanson JE, O'Hara P, Farkas LF, Nair R (1993): Anthropometric craniofacial pattern profiles in Down syndrome. Am J Med Genet 47:748-752.
6. Allanson JE (1996): Objective techniques for craniofacial assessment: What are the choices? Am J Med Genet (this issue).
7. Cole TRP, Hughes HE (1990): Sotos syndrome. J Med Genet 27: 571-576.
8. Cole TRP, Hughes HE (1994): Sotos syndrome: A Study of the diagnostic criteria and natural history. J Med Genet 31:20-32.
9. Farkas LG (1981): Anthropometry of the Head and Face in Medicine. New York: Elsevier.
10. Farkas LG (1994): "Anthropometry of the Head and Face in Medicine," 2nd edition. New York: Raven Press.
11. Fryns JP (1992): Aarskog syndrome: The changing phenotype with age. Am J Med Genet 43:420-427.
12. Garn SM, Smith BH, Lavelle M (1984): Applications of pattern profile analysis to malformations of the head and face. Radiology 150: 683-190.
13. z. Am J Radiol 144:365-369.
14. Hughes-Benzie RM, Hunter AGW, Allanson JE, Mackenzie A (1992): Detailed study of an extended family with Simpson-Golabi-Behmel syndrome. Proc Greenwood Genet Cen 11:109.
15. Hunter AGW, Allanson JE (1994): A followup study of patients with Beckwith-Wiedemann syndrome with emphasis on the change in facial appearance over time. Am J Med Genet 51:102-107.
16. Lopez-Rangel E, Maurice M, McGillivray B, Friedman JM (1992): Williams syndrome in adults. Am J Med Genet 44:720-729.
17. Meaney FJ, Farrer LA (1986): Clinical anthropometry and medical genetics: A compilation of body measurements in genetic and congenital disorders. Am J Med Genet 25:343-359.
18. Porteous MEM, Goudie DR (1991): Aarskog syndrome. J Med Genet 28:44-47.
19. Stevenson RE, Schwartz CE, Wilroy RS, Pasteris NG, Gorski JL (1995): Aarskog-Scott syndrome: phenotype evolution, confirmation of linkage, and gene analysis. Proc Greenwood Gen Ctr 14:47.
20. Ward RE, Bixler D (1987): Anthropometric analysis of the face in hypohidrotic ectodermal dysplasia: A family study. Am J Phys Anthropol 74:453-458.
21. Ward RE, Escobar LF, Carlin ME, Haines JL (1990): Quantitative analysis of the face in the Beckwith Wiedemann syndrome and detection of minimally affected gene carriers. Am J Hum Genet 47:82A.