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Immunodeficiency Type 17
Deal
Immunodeficiency type 17 is a rare disease where part of the immune system does not work properly from birth. In this condition, a gene called CD3G is changed (mutated). This gene helps T cells make ...
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Combined Immunodeficiency Due to CD3-Gamma (CD3γ) Deficiency
Deal
Combined immunodeficiency due to CD3-gamma (CD3γ) deficiency is a very rare, inherited disease of the immune system. In this condition, a small protein called CD3-gamma, which sits on the surface of ...
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Galactosialidosis
Deal
Galactosialidosis is a very rare genetic disease in which the “recycling centres” inside cells, called lysosomes, do not work properly. In healthy people, lysosomes use special proteins called ...
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Combined Deficiency of Sialidase and Beta-Galactosidase
Deal
Combined deficiency of sialidase and beta-galactosidase is a rare inherited disease where two important “clean-up” enzymes inside the cell do not work properly. Doctors usually call this condition ...
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Familial Multiple Coagulation Factor Deficiency
Deal
Familial multiple coagulation factor deficiency is a group of rare inherited bleeding disorders where a person has low levels of two or more blood-clotting proteins at the same time. These proteins ...


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Professor at UCLA School of Medicine
Neurology content on RxHarun.com is well‑structured, with easy‑to‑follow diagrams and patient‑friendly language. I would recommend adding more video animations for complex topics like synaptic transmission.
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Professor at UCLA School of Medicine
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Wills Eye Hospital
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