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The Kleberg Cytogenetics Laboratory offers chromosome analysis on blood, amniotic fluid, chorionic villus, and tissue biopsy specimens. Reasons for Referral:Chromosome analysis is indicated for individuals with any of the following: multiple congenital anomalies, mental retardation, developmental delay, dysmorphic features, sexual ambiguity, multiple miscarriages, infertility, fetal demise, and gamete donor screening. For prenatal cases, chromosome analysis is indicated for advanced maternal age, family history of genetic disease or chromosome abnormality, abnormal maternal serum screening and abnormal ultrasound findings. Testing Methodology:Standard methodology is used for G-banded chromosome analysis and includes high-resolution analysis for all blood specimens. Specimen Requirements:Postnatal (whole
blood in sodium heparin (green-top) tubes): Prenatal: Tissue Biopsy: Shipping and Handling:All tubes must be labeled with the patient's testname and date of birth, and a completed requisition form must accompany each sample. If the laboratory is billing the patient's insurance, please enclose a copy of the insurance card. Ship specimens for overnight delivery at ambient temperature. Please notify the laboratory of incoming samples. Turnaround Time:Postnatal: Prenatal: Tissue Biopsy: CPT Codes and Prices:AFAFP: 82106 Forms: >> Cytogenetics
Requisition Test Codes:AFAFP: 8501 |