Genetics Center Celebrates 36th Anniversary!
Genetics Center is proud to announce that July marks 36 years of genetics service. We are proud to have provided our community with compassionate patient care and excellence in laboratory services throughout these years. Genetics Center would like to thank our referring physicians and patients for being…
July is National Cleft & Craniofacial Awareness & Prevention Month
Each year in the United States, thousands of infants are born with orofacial clefts or other craniofacial conditions that can include cleft lip with or without cleft palate, craniosynostosis and microtia/anotia, among others. These orofacial findings can be hereditary, and comprehensive medical genetics evaluation and…
Genetics Center is proud to be a sponsor of the 2021 Walk for Victory!
Saturday, May 22nd, the Marfan Foundation’s annual Walk for Victory in Southern California will take place virtually. This event raises awareness and funds to support patients and families affected by Marfan syndrome and other connective tissue conditions. Marfan syndrome is an autosomal dominant connective tissue…
May is Cystic Fibrosis Awareness Month
Cystic Fibrosis (CF) is a life long illness that causes lung infections and breathing difficulty. While it is seen most commonly in individuals of European, Caucasian, or Jewish descent, individuals of any ancestry may be affected with this condition. In order to inherit CF, both…
September is Ovarian Cancer Awareness Month & Blood Cancer Awareness Month
Genetic testing is an essential part of early detection and care of Ovarian Cancer and the management of Blood Cancers. The general population lifetime risk for ovarian cancer is 1-2%, and 5-10% of ovarian cancer is due to a hereditary predisposition. Genetics Center performs tests…
August is Spinal Muscular Atrophy (SMA) Awareness Month
SMA is a genetic condition characterized by weakness of the skeletal and respiratory muscles which can present as early as in the womb or present during early or later childhood, and even sometimes during adulthood. This condition is caused by a deletion in both copies…