Torn Frenulum

The frenulum is a small band of tissue that connects the tongue to the floor of the mouth. It plays a crucial…

IGHMBP2 gene

The IGHMBP2 gene encodes a protein called immunoglobulin mu-binding protein 2 (IGHMBP2). This protein plays a crucial role in the survival and…

Vohwinkel syndrome

Vohwinkel syndrome, also known as Vohwinkel syndrome with mutilating keratoderma, is a rare genetic condition characterized by the presence of tight skin…

HJV gene

The HJV gene, also known as hemojuvelin gene (HFE2), is a key gene involved in the regulation of iron homeostasis. Mutations in…

ARMC5 gene

The ARMC5 gene, also known as armadillo repeat containing 5, is a gene that encodes a protein involved in the regulation of…

TNNT2 gene

TNNT2 gene The TNNT2 gene, also known as the troponin T2, cardiac type gene, helps in the production of proteins that are…

Oculocutaneous albinism

Oculocutaneous albinism is a rare genetic condition that affects the pigmentation of the skin, hair, and eyes. It is characterized by a…