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  2. 13q deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/13q_deletion_syndrome

    13q deletion syndrome is a rare genetic disease caused by the deletion of some or all of the large arm of human chromosome 13. Depending upon the size and location of the deletion on chromosome 13, the physical and mental manifestations will vary. It has the potential to cause intellectual disability and congenital malformations that affect a ...

  3. Chromosome 13 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_13

    Chromosome 13 is one of the 23 ... Partial monosomy 13q is a rare chromosomal disorder that results when a piece of the long arm (q) of chromosome 13 is missing ...

  4. Partial monosomy 13q - Wikipedia

    en.wikipedia.org/wiki/Partial_monosomy_13q

    Partial monosomy of chromosome 13q is a monosomy that results from the loss of all or part of the long arm of chromosome 13 in human beings. It is a rare genetic disorder which results in severe congenital abnormalities which are frequently fatal at an early age. Up until 2003, more than 125 cases had been documented in medical literature. [1]

  5. Chromosome abnormality - Wikipedia

    en.wikipedia.org/wiki/Chromosome_abnormality

    When the chromosome's structure is altered, this can take several forms: [16] Deletions: A portion of the chromosome is missing or has been deleted. Known disorders in humans include Wolf–Hirschhorn syndrome, which is caused by partial deletion of the short arm of chromosome 4; and Jacobsen syndrome, also called the terminal 11q deletion ...

  6. This Florida resort gives critically ill children the chance ...

    www.aol.com/florida-resort-gives-critically-ill...

    Elliot was born with a cleft lip, cleft palate, congenital heart defect and chromosome disorder that is so rare, his mom, Jessica Kostelak, said it doesn't even have a name.

  7. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.

  8. Patau syndrome - Wikipedia

    en.wikipedia.org/wiki/Patau_syndrome

    Patau syndrome is a syndrome caused by a chromosomal abnormality, in which some or all of the cells of the body contain extra genetic material from chromosome 13. The extra genetic material disrupts normal development, causing multiple and complex organ defects.

  9. Jack The Ripper’s Identity Revealed After 130 Years ... - AOL

    www.aol.com/lifestyle/took-them-137-years-jack...

    Scientists have doubts about the study results, need genetic sequences to be sure. ... James MacKelan tweet expressing relief for closure in Jack the Ripper case, dated February 13, 2025.