Cerebral gigantism-jaw cysts syndrome is an extremely rare birth (congenital) condition in which a child has very fast body and head growth (cerebral gigantism) together with special cysts in the jaw ...
Cerebellar-facial-dental syndrome (CFDS) is a very rare genetic condition that affects brain development, face shape, and teeth. It is a neurodevelopmental disorder, which means it starts before ...
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural deafness syndrome is a very rare inherited brain and nerve disorder. Doctors often call it CAPOS syndrome (from the first letters of ...
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 (weak or absent reflexes), ...
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome is usually called CAPOS syndrome. It is a very rare genetic brain and nerve disorder. It affects balance and ...
Cerebellar ataxia with bilateral vestibular syndrome means that two balance systems are damaged at the same time. The first system is the cerebellum, a part of the brain that helps control balance, ...
Cerebellar ataxia with bilateral vestibulopathy syndrome is a rare brain and inner-ear disorder where two main problems happen together: damage in the cerebellum (the part of the brain that controls ...
Central nervous system calcification–deafness–tubular acidosis–anemia syndrome is a very rare inherited disorder that affects the brain and spinal cord, hearing, kidney acid control, and red blood ...
Oral myiasis is an infection in the mouth caused by the larvae (baby stage) of certain flies. These tiny larvae live in soft tissues of the mouth, such as the gums, cheeks, lips, or tongue, and feed ...
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 ...
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-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), ataxia (poor ...
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 defects, special ...
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 of ...
Acute gangrenous stomatitis is a very fast-moving infection that destroys the mouth and face. It usually begins as sore, bleeding gums, then the tissues of the cheek, lips, and jaw die and break ...
Necrotizing ulcerative stomatitis is a severe mouth infection. The soft lining of the mouth dies in patches, and deep ulcers form. These ulcers can cut across the gums, cheeks, and other mouth ...
Gangrenous stomatitis—better known today as noma or cancrum oris—is a fast-moving infection that destroys the gums, cheeks, lips, and sometimes the nose and jaw. It mainly affects children who are ...
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 gums. In a few days it can destroy soft tissue, ...
Stomatopyrosis means a constant or frequent burning, scalding, or tingling feeling in your mouth even though the lining of the mouth looks normal. The burning is usually felt on the tongue but can ...
Stomatodynia means a long-lasting burning, scalding, or tingling pain inside the mouth even though the mouth looks normal when a dentist or doctor examines it. The tongue is the most common place, ...
