Search Results

Children with mucopolysarcharidosis type I (MPS I) have an abnormal accumulation of complex sugars in their cells, which affects many of the systems in their bodies.

A malunion fracture is a broken bone that heals abnormally.

Mucolipidosis III (ML III) is a rare, inherited disorder in which genetic variations disrupt the normal activity of lysosomes in human cells.

Metatarsus adductus (metatarsus varus) is a common deformity that causes the front half of the foot to turn inward.

Metopic synostosis (trigonocephaly or metopic suture craniosynostosis) is a type of craniosynostosis, when a developing infant’s skull fuses too early.

In microcephaly, the brain develops abnormally, causing the head to be much smaller than expected for the child's age.

Microvillus inclusion disease (MVID) is a rare genetic disease of the intestine that causes severe diarrhea and an inability to absorb nutrients.

Children with movement disorders have involuntary movements or trouble moving in the way they intend to.

Muscular dystrophy is a general name for a group of rare diseases that cause muscle weakness. It is caused by mutations in certain genes.

A malignant fibrous histiocytoma is a type of cancerous tumor that can start in bone or in the soft tissues that connect, support, or surround organs and other body parts.