KIF11 Gene Microcephaly with or without Chorioretinopathy Lymphedema or Mental Retardation MCLMR Genetic Test sale cost 4400 AED
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KIF11 Gene Microcephaly with or without Chorioretinopathy Lymphedema or Mental Retardation MCLMR Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The KIF11 Gene Microcephaly with or without Chorioretinopathy, Lymphedema, or Mental Retardation (MCLMR) Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the KIF11 gene. These mutations are associated with a rare genetic disorder that manifests as a spectrum of symptoms, including microcephaly (a condition where a baby’s head is significantly smaller than expected), potential vision problems due to chorioretinopathy, lymphedema (swelling due to lymphatic system blockages), and in some cases, mental retardation. The test, priced at 4400 AED, provides crucial information for the diagnosis and management of this condition, enabling targeted interventions and support for affected individuals and their families.

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KIF11 Gene Microcephaly with or without chorioretinopathy Lymphedema or Mental retardation MCLMR Genetic Test

Test Name: KIF11 Gene Microcephaly with or without chorioretinopathy Lymphedema or Mental retardation MCLMR Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test type: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for KIF11 Gene Microcephaly with or without chorioretinopathy, Lymphedema, or Mental retardation, MCLMR NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KIF11 Gene Microcephaly with or without chorioretinopathy, Lymphedema, or Mental retardation, MCLMR NGS Genetic DNA Test gene KIF11

Test Details:

The KIF11 gene is associated with a genetic condition known as Microcephaly with or without chorioretinopathy, Lymphedema, or Mental retardation (MCLMR). This condition is characterized by a combination of microcephaly (abnormally small head size), chorioretinopathy (a disorder affecting the retina and choroid in the eye), lymphedema (swelling of the limbs due to fluid buildup), and intellectual disability.

The MCLMR NGS genetic test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze the KIF11 gene for any mutations or variations. This test can help in confirming a diagnosis of MCLMR and providing information about the specific genetic variant causing the condition.

Genetic testing for MCLMR can be beneficial for individuals suspected to have the condition, as it can provide a definitive diagnosis, inform prognosis, and guide appropriate medical management and genetic counseling. It can also be useful for family members of affected individuals, as it can help determine their risk of having a child with MCLMR.

It is important to consult with a healthcare professional or a genetic counselor to understand the implications, limitations, and potential benefits of genetic testing for MCLMR before undergoing the test.

Test Name KIF11 Gene Microcephaly with or without chorioretinopathy Lymphedema or Mental retardation MCLMR 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for KIF11 Gene Microcephaly with or without chorioretinopathy, Lymphedema, or Mental retardation, MCLMR NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KIF11 Gene Microcephaly with or without chorioretinopathy, Lymphedema, or Mental retardation, MCLMR NGS Genetic DNA Test gene KIF11
Test Details

The KIF11 gene is associated with a genetic condition known as Microcephaly with or without chorioretinopathy, Lymphedema, or Mental retardation (MCLMR). This condition is characterized by a combination of microcephaly (abnormally small head size), chorioretinopathy (a disorder affecting the retina and choroid in the eye), lymphedema (swelling of the limbs due to fluid buildup), and intellectual disability.

The MCLMR NGS genetic test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze the KIF11 gene for any mutations or variations. This test can help in confirming a diagnosis of MCLMR and providing information about the specific genetic variant causing the condition.

Genetic testing for MCLMR can be beneficial for individuals suspected to have the condition, as it can provide a definitive diagnosis, inform prognosis, and guide appropriate medical management and genetic counseling. It can also be useful for family members of affected individuals, as it can help determine their risk of having a child with MCLMR.

It is important to consult with a healthcare professional or a genetic counselor to understand the implications, limitations, and potential benefits of genetic testing for MCLMR before undergoing the test.

SKU: TEST-4242 Category:

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