Malaria Tests
If you have symptoms of malaria or if you’ve traveled to parts of the world where malaria is common, it’s important to…
Yuan-Harel-Lupski syndrome
Yuan-Harel-Lupski syndrome, also known as Potocki-Lupski syndrome, is a rare genetic disorder caused by duplications in a specific region of chromosome 17.…
Lung Function Tests
When people have normal lung function, they don’t really think about it. Breathing is just something that happens automatically, without much effort…
Enlarged parietal foramina
Enlarged parietal foramina, also known as foramen parietal occultum, is a rare genetic condition. It is inherited in an autosomal dominant manner,…
Mucolipidosis III gamma
Mucolipidosis III gamma, also known as Raas-Rothschild syndrome, is a rare autosomal recessive lysosomal storage disorder. This condition is caused by mutations…
SALL4 gene
The SALL4 gene is a genetic variant that plays a crucial role in various developmental processes in the human body. It has…
Fanconi anemia
Fanconi Anemia (FA) is a rare genetic condition that affects both males and females. It is characterized by a pattern of bone…
Central precocious puberty
Central precocious puberty (CPP) is a condition in which girls experience early puberty, typically before the age of 8. It is characterized…
Ring chromosome 14 syndrome
The ring chromosome 14 syndrome is a rare genetic condition that affects the structure and function of chromosome 14. This condition is…