Dismiss Modal

Diagnosis

Estudios para la Detección de Defectos Congénitos

Choose a preferred language

Existe una diversidad de pruebas que pueden realizarse para determinar si un niño padece un defecto congénito genético. En el directorio que aparece a continuación se enumeran algunas de ellas, para las cuales le proveemos una breve descripción.

Los Estudios Cromosómicos: el Cariotipo, el Bandeo Extendido, la Hibridación Fluorescente In Situ (FISH), y Análisis de Microarreglo Cromosómico

Los Estudios para Defectos en un único Gen: ADN (Directos e Indirectos)

Featured in

© 2000-2025 The StayWell Company, LLC. Todos los derechos reservados. Esta información no pretende sustituir la atención médica profesional. Sólo su médico puede diagnosticar y tratar un problema de salud.
Related Articles
Read article
Read article
Genetic and Congenital Conditions
Evaluating a Child for Birth Defects

Detailed information on evaluating a child for birth defects

Read article
Read article
Genetic and Congenital Conditions
Medical Genetics: Chromosome Studies

When a chromosome is abnormal, it can cause health problems in the body. Tests called studies can look at chromosomes to see what type of problem a person has.

Read article
Read article
Genetic and Congenital Conditions
Medical Genetics: DNA Studies for Single Gene Defects

To look for single gene defects, healthcare providers look at the DNA to see if it has any errors in it. Errors are known as mutations.

Read article
Read article
Topic Index

Detailed information on medical genetics, including chromosome abnormalities, single gene defects, multifactorial inheritance, teratogens, and non-traditional inheritance