Ophthalmomyiasis (also called ocular myiasis) means fly larvae (maggots) get into or onto the eye area. The larvae can stay on the surface (like the ...

Cerebral myiasis means fly larvae (maggots) infest tissue in or around the brain. It is extremely rare. In most reported cases, larvae get access through an ...

Urogenital myiasis (also called genitourinary myiasis) is a rare condition where fly larvae (immature flies) are found in or near the urinary or genital area, ...

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 ...

Nasal myiasis is a condition where fly larvae (maggots) live and grow inside the nose or nearby sinuses. The flies lay eggs around the nostrils or in nasal ...

Aural myiasis (also called otomyiasis) means fly larvae (maggots) are living in the ear canal, and sometimes they can reach the middle ear if the eardrum is ...

Cavitary myiasis is a parasitic disease where fly larvae (maggots) live and grow inside natural body openings instead of on the skin surface. These openings ...

Macrocystic lymphatic malformation (macrocystic LM) is a type of lymphatic malformation, which means it is an abnormal cluster of lymph vessels and ...

Macrocystic lymphangioma is an old name for a macrocystic lymphatic malformation. It is a benign (non-cancerous) lump made of many large, fluid-filled spaces ...

A cavernous lymphatic malformation (CLM) is a slow-flow vascular malformation made of abnormally formed lymphatic channels and cyst-like spaces (often many ...

Cavernous lymphangioma is a benign (non-cancer) growth made of abnormally wide lymphatic vessels deep in the skin and soft tissues. It belongs to the family of ...

Sacral agenesis syndrome is a rare birth condition where the lowest part of the spine (the sacrum and often the coccyx and lower lumbar vertebrae) does not ...

Caudal dysplasia sequence (also called caudal regression syndrome) is a rare birth condition in which the lower part of the baby’s body does not form normally ...

Caudal dysgenesis syndrome (CDS) is a rare birth defect where the lower part of the baby’s spine and nearby organs do not form in the usual way during very ...

Caudal regression sequence is a rare birth condition where the lower part of a baby’s spine and nearby organs do not form completely in the womb. It mainly ...

Split notochord syndrome (SNS) is a very rare birth defect that affects the early “midline” of the baby’s body, especially the spine, spinal cord, and nearby ...

Dipygus is an extremely rare birth defect where the lower part of the body is partly or completely doubled, usually with two pelvises and extra legs that grow ...

Cataract 46 juvenile-onset is a rare inherited eye disease where the clear lens inside the eye slowly becomes cloudy in childhood, usually between about 3 and ...

CPT1A disorder (also called CPT I deficiency) is a genetic problem with fat burning. The CPT1A enzyme sits on the outer wall of the mitochondria in liver and ...

CPT1A (Carnitine Palmitoyltransferase I-A) Deficiency is a genetic disorder in which the liver enzyme CPT1A does not work well. This enzyme sits on the outer ...