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Rare Disease Database

2 Search Results for: MKS

NORD Rare Disease Database

Meckel Syndrome

Summary Meckel syndrome is a rare inherited disorder characterized by abnormalities affecting several organ systems of the body. Three classic symptoms are normally...

Also known as: dysencephalia splanchnocystica, Gruber syndrome, Meckel-Gruber syndrome, MES, MKS

NIH GARD Information

Meckel syndrome

Meckel syndrome is a very severe disorder that is characterized by multiple cysts on the kidneys, protrusion of a portion of the brain through an...