LBR Gene Greenberg skeletal dysplasia Genetic Test

Test Details

Skeletal dysplasia refers to a group of genetic disorders that affect the growth and development of bones. These disorders can result in abnormal bone shape, size, and density, leading to various skeletal abnormalities.

NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology that allows for the analysis of multiple genes simultaneously. NGS genetic testing is used to identify genetic variations or mutations that may be associated with certain conditions or diseases, including skeletal dysplasias.

LBR (Lamin B receptor) is a gene that is associated with a specific type of skeletal dysplasia called Greenberg skeletal dysplasia. Mutations in the LBR gene can cause this rare genetic disorder, which is characterized by severe skeletal abnormalities, growth retardation, and other health issues.

NGS genetic testing can be used to analyze the LBR gene and identify any mutations or variations that may be present. This can help in confirming a diagnosis of Greenberg skeletal dysplasia and providing genetic counseling for affected individuals and their families.

Overall, NGS genetic testing of the LBR gene can play a crucial role in the diagnosis and management of skeletal dysplasias, including Greenberg skeletal dysplasia.

Test Name: LBR Gene Greenberg skeletal dysplasia Genetic Test

Components:

• Price: 4400.0 AED

Sample Condition:

• Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery:

• 3 to 4 Weeks

Method:

• NGS Technology

Test Type:

• Osteology Dermatology Immunology Disorders

Doctor:

• Dermatologist

Test Department:

• Genetics

Pre Test Information:

• Clinical History of Patient who is going for LBR Gene Greenberg skeletal dysplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LBR Gene Greenberg skeletal dysplasia NGS Genetic DNA Test gene LBR