Albinism is a rare genetic condition caused by mutations of certain genes that affect the amount of melanin your body produces. Melanin controls the pigmentation (color) of your skin, eyes, and hair.People with albinism have extremely pale skin, eyes, and hair. They are at an increased risk of vision, skin, and social issues; the patients aren't born with the usual amount of melanin pigment.Melanin is a ch  Read More

Ganglioside sialidase deficiency is also known as Sialoglycosphingolipids/ Mucolipidosis IV.They carry one or more than one sialic residue. This is a very rare metabolic disorder.It may arise due to a deficiency of transport channel receptor protein. If this disease becomes severe, it is called typical mucolipidosis IV; if it is mild and not that severe, it is called atypical mucolipidosis IV.Medication  Read More

The precise cause for Ito hypomelanosis is unknown.Genetic mosaicism and spontaneous gene mutations are linked to several occurrences.The term "genetic mosaicism" refers to people who established two separate cell lines in their bodies as a result of a gene mutation that happened during embryonic development. •Chromosome discrepancies exist between the two cell lines (chromosomal mosaicism).  Read More