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At Dr. StemCellsThailand, we are dedicated to advancing the field of regenerative medicine through innovative cellular therapies and stem cell treatments. With over 20 years of experience, our expert team is committed to providing personalized care to patients from around the world, helping them achieve optimal health and vitality. We take pride in our ongoing research and development efforts, ensuring that our patients benefit from the latest advancements in stem cell technology. Our satisfied patients, who come from diverse backgrounds, testify to the transformative impact of our therapies on their lives, and we are here to support you on your journey to wellness.

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Category: Hereditary Diseases

Tay-Sachs disease (TSD) is a rare, inherited neurodegenerative disorder caused by mutations in the HEXA gene on chromosome 15, which encodes the alpha subunit of the enzyme hexosaminidase A (HexA). This enzyme is essential for breaking down GM2 ganglioside, a fatty substance in nerve cells. Deficiency of HexA leads to the accumulation of GM2 ganglioside in the brain and spinal cord, causing progressive neuronal damage and death.

Tay-Sachs Disease

Tay-Sachs disease (TSD) is a rare, inherited neurodegenerative disorder caused by mutations in the HEXA gene on chromosome 15, which encodes the alpha subunit of the enzyme hexosaminidase A (HexA). This

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Marfan syndrome is a genetic disorder affecting connective tissue, caused primarily by mutations in the FBN1 gene, which encodes fibrillin-1, a protein essential for the formation of microfibrils that provide strength and elasticity to connective tissues126. The condition is inherited in an autosomal dominant pattern, meaning a single copy of the altered gene is sufficient to cause the disorder123. About 25% of cases arise from new (de novo) mutations without a family history123.

Marfan Syndrome

Marfan syndrome is a genetic disorder affecting connective tissue, caused primarily by mutations in the FBN1 gene, which encodes fibrillin-1, a protein essential for the formation of microfibrils that provide strength

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Hereditary disorders, also known as genetic disorders, are health conditions caused by abnormalities in an individual's genetic material—either in their DNA sequence or chromosome structure—that are passed down from parents to offspring. These disorders can manifest at birth or develop later in life and vary widely in severity and symptoms.

Hereditary Disorders

Hereditary disorders, also known as genetic disorders, are health conditions caused by abnormalities in an individual's genetic material—either in their DNA sequence or chromosome structure—that are passed down from parents to

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