Branchiogenic Hearing Loss Syndrome
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DefinitionBranchiootorenal (BOR) syndrome is a rare genetic disorder that affects various parts of the body, including the ears, kidneys, and neck. This article aims to provide...
DefinitionBurn-McKeown syndrome is a very rare genetic condition present from birth. Children with this syndrome usually have blocked or very narrow back parts of the nose...
DefinitionBurning Mouth Syndrome (BMS) is a condition that can cause discomfort and pain? in the mouth, often described as a burning or scalding sensation. This article...
DefinitionBurning mouth syndrome is long-lasting mouth pain? that feels like burning, scalding, tingling, or rawness even though the mouth looks normal. It often affects the tongue...
DefinitionCancrum oris, also called noma, is a very fast, severe infection? that eats the mouth and face. It usually starts inside the mouth as sore, swollen...
DefinitionCAPOS syndrome is a very rare genetic brain and nerve disease. The name CAPOS comes from five main problems: Cerebellar ataxia (poor balance and coordination), Areflexia...
DefinitionCardiac anomalies–developmental delay–facial dysmorphism syndrome” is a rare genetic condition. Children with this condition often have heart problems that are present at birth, a slower pace...
DefinitionCardiofaciocutaneous syndrome is a rare genetic condition. It mainly affects the heart (cardio-), the face (facio-), and the skin and hair (cutaneous). Children usually have heart...
DefinitionCataract-ataxia-deafness syndrome is an extremely rare genetic disorder in which a person has three main problems together: cataracts present from birth (clouding of the eye lenses),...
DefinitionCataract-ataxia-hearing loss syndrome (often called cataract-ataxia-deafness syndrome) is an extremely rare genetic disorder. Only a very small number of patients (two sisters in one family) have...
DefinitionCataract-hearing loss-hypogonadism syndrome (usually called cataract-deafness-hypogonadism syndrome) is an extremely rare genetic disease. It was first reported in three brothers from one family. The main features...