Jacobsen Syndrome (11q Deletion, or 11q-) is a rare chromosomal abnormality which affects perhaps one child in 100,000 in which a portion of the 11th chromosome is missing. It was discovered by Dr. P. Jacobsen in 1973. At that time, the disease was named "Jacobsen Syndrome."- Category ID : 75661
Provides information on this condition caused by a loss of genetic material from chromosome 11, its features, inheritance and other sources of information.
Factsheet on this rare chromosome disorder that affects multiple aspects of physical and mental development, its signs and symptoms, management and prognosis.