Genetic Counselling
How does Genetic counselling help you?
Genetic Counselling helps in
- Helps in the root cause diagnosis of the genetic condition
- Helps in the management of the case by providing elaborate information on disease progression
- Advises on the best-suited genetic test for the case which has the highest possibility of providing accurate diagnosis
- Identifies the chances of conceiving a child with a genetic disorder and allows preventive management
- Explain the advantages and limitations of invasive procedures performed during pregnancy
- Elaborates on options for testing embryos for IVF conceptions
- Identifies risk for extended family members developing the genetic condition diagnosed in the family
- Based on the genetic data of the patient, personalised treatment and management plans are shared with physicians
- Answers frequently asked questions of patients and their family members
Genetic & genomic
counselling - book a counselling
Mother and Child Genomics Expert Counselling
Recurrent pregnancy loss, abnormal ultrasound findings, high-risk screening results, child with developmental delay, autism, mental retardation, or other genetic disorder, family history, consanguinity
Speciality Genomics Expert Counselling
Epilepsy, Autism, Developmental delay, ambiguous genitalia, Facial dysmorphism, cardiac defects, endocrinological defects, Skeletal and Muscular defects, familial cancers, eye defects, hearing loss, dermatological disorders.
Fertility Genomics Expert Counselling
Male or female infertility, recurrent implantation failures, poor response to ovarian stimulation, PCOD, fertilisation failure, recurrent pregnancy loss, azoospermia, sperm defects, multiple IUI or IVF or ICSI cycle failures
Personal Genomics Expert Counselling
Genetics based personalised wellness plans for individualised nutrition, fitness regime, skin care, prevention of lifestyle disorders, efficacy of anti-aging and longevity treatments, drug response, gut health, behavioural conditions.
What happens in a genetic counselling session?
01 Examining medical records and gathering case history
02 03 Three-generation pedigree to understand disease inheritance pattern
04 Extraction of data from genetic database resources
05 Explain progression, onset and recurrence risk of the condition
06 Detailed letter and call to the physician for discussion
