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Bare Lymphocyte Syndrome

Bare Lymphocyte Syndrome

  Bare Lymphocyte Syndrome (BLS) is a rare, genetic immune disorder that affects the body’s ability to produce and respond to certain types of white blood cells. It is primarily caused by a mutation in the RAG1 or RAG2 gene. This mutation affects the...
Generalized Essential Telangiectasia

Generalized Essential Telangiectasia

  Generalized essential telangiectasia (G.E.T) is a rare, chronic skin disorder that is characterized by the development of dilated capillaries on the surface of the skin. It is sometimes also referred to as “spider veins” or...
Pregnancy Tumor

Pregnancy Tumor

  H Pregnancy tumors are a rare type of tumor that can develop during pregnancy. They are often benign, but they can be cancerous in some cases. Pregnancy tumors can affect any organ of the body, but they are most commonly found in the breast or reproductive...
Hereditary Progressive Mucinous Histiocytosis

Hereditary Progressive Mucinous Histiocytosis

  Hereditary Progressive Mucinous Histiocytosis (HPMH) is a rare genetic disorder characterized by the buildup of mucous-producing cells in various organs and tissues. It is an autosomal dominant condition, meaning it can be inherited from a single parent....
Focal Dermal Hypoplasia

Focal Dermal Hypoplasia

  Focal Dermal Hypoplasia (FDH), also known as Goltz Syndrome, is a rare genetic disorder that affects the skin, bones, and teeth. It is characterized by malformation of the dermis, which is the middle layer of the skin. FDH can lead to a variety of birth...
Xanthelasma Treatment