Cerebral Gigantism-Jaw Cysts Syndrome
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-jaw cysts syndrome is an extremely rare birth (congenital) condition in which a child has very fast body and head growth…
Cerebellar-facial-dental syndrome (CFDS) is a very rare genetic condition that affects brain development, face shape, and teeth. It is a neurodevelopmental disorder,…
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…
CAPOS syndrome is a very rare genetic brain and nerve disease. The name CAPOS comes from five main problems: Cerebellar ataxia (poor…
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.…
Cerebellar ataxia with bilateral vestibular syndrome means that two balance systems are damaged at the same time. The first system is the…
Cerebellar ataxia with bilateral vestibulopathy syndrome is a rare brain and inner-ear disorder where two main problems happen together: damage in the…
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…
Oral myiasis is an infection in the mouth caused by the larvae (baby stage) of certain flies. These tiny larvae live in…
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…
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…
Cataract-ataxia-deafness syndrome is an extremely rare genetic disorder in which a person has three main problems together: cataracts present from birth (clouding…
Cardiofaciocutaneous syndrome is a rare genetic condition. It mainly affects the heart (cardio-), the face (facio-), and the skin and hair (cutaneous).…
Cardiac anomalies–developmental delay–facial dysmorphism syndrome” is a rare genetic condition. Children with this condition often have heart problems that are present at…
Acute gangrenous stomatitis is a very fast-moving infection that destroys the mouth and face. It usually begins as sore, bleeding gums, then…
Necrotizing ulcerative stomatitis is a severe mouth infection. The soft lining of the mouth dies in patches, and deep ulcers form. These…
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…
Cancrum oris, also called noma, is a very fast, severe infection that eats the mouth and face. It usually starts inside the…
Stomatopyrosis means a constant or frequent burning, scalding, or tingling feeling in your mouth even though the lining of the mouth looks…
Stomatodynia means a long-lasting burning, scalding, or tingling pain inside the mouth even though the mouth looks normal when a dentist or…