Chin-To Fong, M.D.

See information for Patients. Viewing information for Researchers.

Contact

University of Rochester
School of Medicine and Dentistry
601 Elmwood Ave, Box 777
Rochester, New York 14642

Office: 585 275-5857

Fax: 585 273-1018

Portrait

Dr. Fong's primary research interest is Genetics of orofacial clefts. Cleft lip and palate is a common birth defect that affects one in 700 children in the U. S. and around the world. Children with this birth defect face multiple challenges, such as feeding difficulty, hearing impairment, speech defects and many dental abnormalities. These problems, along with the cosmetic changes associated with the clefts, often result in life-long physical, educational and psychological handicaps. Caring of these children thus requires a team approach over long periods of time.

Cleft lip and palate is a familial trait, but the genetic factors that result in this abnormality have not been clearly identified. Recent calculations have led to the belief that as many as a couple dozen genetic factors may act together to cause cleft lip and palate, with a few of the factors being more important than the rest. Moreover, there is convincing evidence that environment factors, such as cigarette smoking by the pregnant mother, play a role in the development of cleft lip and palate in the fetus.

In these situations, the environmental and genetic factors act together to cause the birth defect. Therefore, cleft lip and palate is considered a multifactorial genetic disorder. The work in our laboratory is focused on finding the genetic factors for cleft lip and palate through linkage disequilibrium analyses. We believe that better treatment and prevention of cleft lip and palate will come from a better understanding of these genetic and environmental factors.

Specialty

Genetics

Current Appointments

Education
MD Medicine Harvard Medical School (Harvard-MIT Division of Health Science & Technology) 1981
SB Biology Massachusetts Institute of Technology 1978
SM Biology Massachusetts Institute of Technology 1978
Post-Doctoral Training & Residency
Medical Genetics Fellowship, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 1984 - 1987
Residency in Pediatrics, St. Louis Children's Hospital, St. Louis, MO 1981 - 1984
Board Certifications
American Board of Clinical Biochemical Genetics 1987 - Present
American Board of Clinical Genetics 1987 - Present
American Board of Medical Genetics 1987 - Present
American Board of Pediatrics 1986 - Present
Recent Journal Articles
Showing the 5 most recent journal articles. (27 available)
Yoon YJ; Perkiomaki MR; Tallents RH; Barillas I; Herrera-Guido R; Fong CT; Kyrkanides S. "Transverse craniofacial features and their genetic predisposition in families with nonsyndromic unilateral cleft lip and palate." The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. 2004; 41(3):256-61.
Perkiomaki MR; Yoon YJ; Tallents RH; Barillas I; Herrera-Guido R; Moss ME; Fong CT; Kyrkanides S. "Association of distinct craniofacial features in nonsyndromic cleft lip and palate family members." The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. 2003; 40(4):397-402.
Yoon YJ; Perkiomaki MR; Tallents RH; Barillas I; Herrera-Guido R; Fong CT; Kyrkanides S. "Association of nasomaxillary asymmetry in children with unilateral cleft lip and palate and their parents." The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. 2003; 40(5):493-7.
Suzuki T; Li W; Zhang Q; Karim A; Novak EK; Sviderskaya EV; Hill SP; Bennett DC; Levin AV; Nieuwenhuis HK; Fong CT; Castellan C; Miterski B; Swank RT; Spritz RA. "Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene." Nature genetics. 2002; 30(3):321-4. Epub 2002 Feb 11.
Kaczorowski JM; Halterman JS; Spitalnik P; Mannick E; Fong CT; Seaman JM. "Pathology teach and tell: congenital hepatic fibrosis and autosomal dominant polycystic kidney disease." Pediatric pathology & molecular medicine. 2001; 20(3):245-8.