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  2. Jacobsen syndrome - Wikipedia

    en.wikipedia.org/wiki/Jacobsen_syndrome

    Jacobsen syndrome is a rare chromosomal disorder resulting from deletion of genes from chromosome 11 that includes band 11q24.1. It is a congenital disorder . Since the deletion takes place on the q arm of chromosome 11, it is also called 11q terminal deletion disorder. [ 1 ]

  3. Creutzfeldt–Jakob disease - Wikipedia

    en.wikipedia.org/wiki/Creutzfeldt–Jakob_disease

    Creutzfeldt–Jakob disease (CJD), also known as subacute spongiform encephalopathy or neurocognitive disorder due to prion disease, is a fatal neurodegenerative disease. [4] [1] Early symptoms include memory problems, behavioral changes, poor coordination, and visual disturbances. [4]

  4. XYY syndrome - Wikipedia

    en.wikipedia.org/wiki/XYY_syndrome

    XYY syndrome, also known as Jacobs syndrome, is an aneuploid genetic condition in which a male has an extra Y chromosome. [1] There are usually few symptoms. [ 2 ] These may include being taller than average and an increased risk of learning disabilities .

  5. Camptodactyly - Wikipedia

    en.wikipedia.org/wiki/Camptodactyly

    Camptodactyly can be caused by a genetic disorder. In that case, it is an autosomal dominant trait that is known for its incomplete genetic expressivity . This means that when a person has the genes for it, the condition may appear in both hands, one, or neither.

  6. Wolf–Hirschhorn syndrome - Wikipedia

    en.wikipedia.org/wiki/Wolf–Hirschhorn_syndrome

    Wolf–Hirschhorn syndrome (WHS) is a chromosomal deletion syndrome resulting from a partial deletion on the short arm of chromosome 4 [del(4)(p16.3)]. [3] Features include a distinct craniofacial phenotype and intellectual disability .

  7. Machado–Joseph disease - Wikipedia

    en.wikipedia.org/wiki/Machado–Joseph_disease

    Machado–Joseph disease (MJD), also known as Machado–Joseph Azorean disease, Machado's disease, Joseph's disease or spinocerebellar ataxia type 3 (SCA3), is a rare autosomal dominantly inherited neurodegenerative disease that causes progressive cerebellar ataxia, [1] [2] which results in a lack of muscle control and coordination of the upper and lower extremities. [3]

  8. Siblings challenge stereotypes about Down syndrome with funny ...

    www.aol.com/news/siblings-challenge-stereotypes...

    March 21 (3/21) is World Down Syndrome Day, chosen because people with Down Syndrome have three copies of the 21st chromosome instead of the usual two. "Gabe lives his life to the fullest," Nick ...

  9. Cocooning (immunization) - Wikipedia

    en.wikipedia.org/wiki/Cocooning_(immunization)

    The immune system can be compromised by congenital medical conditions, infectious diseases, non-infectious conditions such as cancer, and immunosuppressive medications or treatments (for instance, people with organ transplants take drugs to prevent their immune system from killing the transplant). People who are severely immuno-compromised may ...