Search Results 1-10 of 7848 for Karyotype
Hormone testing. Blood or urine samples can reveal abnormal hormone levels that are a sign of Klinefelter syndrome. Chromosome analysis. Also called karyotype ...
Females with this genetic disorder have three X chromosomes instead of two. Symptoms can be mild or include developmental delays and learning disabilities.
Routine Cytogenetic Analysis. Representative G-banded karyotype. Routine cytogenetic analysis by the Cytogenetics Core requires metaphase slides prepared by ...
This genetic disorder occurs when a male is born with an extra copy of the X chromosome and may result in low testosterone production and infertility.
For example, the core can produce metaphases for cytogenetic analysis or karyotypes from an investigator's cell line of interest. In addition, the core can ...
Detecting chromosome and gene defects; Imaging and karyotyping of specimens; Reporting findings to physicians for diagnosis and treatment. Work environment.
... karyotype to confirm diagnosis. Using a sample of blood, this test analyzes your child's chromosomes. If there's an extra chromosome 21 in all or some cells ...
However, doing a karyotype during pregnancy or after delivery is recommended to confirm the diagnosis. If Turner syndrome is suspected before birth ...
This condition is due to missing part of chromosome 22. It may cause heart issues, thyroid problems, cleft palate, lower immunity and other health problems.
This rare, inherited disease causes a buildup of fatty acids that damages the brain and typically results in muscle control loss, blindness and paralysis.
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