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29 Mar
2024

What is Fragile X syndrome, Symptoms, Diagnosis, and Treatment Options

Fragile X syndrome (FXS) is a genetic disorder that causes a range of developmental and behavioral problems, including learning disabilities, cognitive impairment, and social and emotional difficulties. FXS is caused by mutations in the FMR1 (Fragile X Mental Retardation 1) gene, located on the X chromosome…. Read More »

28 Mar
2024

What is the Lymphedema-distichiasis Syndrome?

Lymphedema-distichiasis syndrome is a rare genetic disorder inherited in an autosomal dominant pattern. It can affect individuals of any racial or ethnic background, and there is no evidence to suggest that it disproportionately affects any specific population. Genetic disorders can occur in individuals regardless of race, and prevalence may vary across populations due to various factors… Read More »

04 May
2023

Genetic Disorders Overview, Risks, Novel Therapies

Genetic disorders are disorders caused by abnormalities in an individual’s DNA or genes, which can be inherited or arise spontaneously. They can be classified based on the type of genetic alteration, such as mutations, deletions, insertions, or chromosomal abnormalities…. Read More »

18 Sep
2017

Albinism Definition Clinical symptoms and Precautions

All about albinism

Albinism is a rare autosomal genetic disorder that is inherited from one generation into another through one recessive gene, it is characterized by abnormal melanocytes. In most cases, albinos live a short life (less than 35 years) and deaths occur due to skin cancers…. Read More »

09 May
2015

Albinism Definition Clinical symptoms and Precautions

All about albinism

Albinism is a rare autosomal genetic disorder that is inherited from one generation into another through one recessive gene, albinism is characterized by abnormal melanocytes (they do not form melanin); In most cases, albinos live a short life (less than 35 years) and deaths occur due to skin cancers…. Read More »

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