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Branchiogenic hearing loss syndrome refers to a group of birth conditions where parts of the neck and ear that grow from the branchial arches (structures that...
Branchiootorenal (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...
Burn-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...
Burning 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...
Burning 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...
Cancrum 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...
CAPOS 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...
Cardiac 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...
Cardiofaciocutaneous 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...
Cataract-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),...
Cataract-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...
Cataract-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...
