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  2. 22q11.2 duplication syndrome - Wikipedia

    en.wikipedia.org/wiki/22q11.2_duplication_syndrome

    The most frequent reported symptoms in patients with 22q11.2 duplication syndrome are intellectual disability /learning disability (97% of patients), delayed psychomotor development (67% of patients), growth retardation (63% of patients) and muscular hypotonia (43% of patients). [ 1 ] However, these are common and relatively non-specific ...

  3. Mutation - Wikipedia

    en.wikipedia.org/wiki/Mutation

    Phenotypes associated with such mutations are most often recessive. Exceptions are when the organism is haploid, or when the reduced dosage of a normal gene product is not enough for a normal phenotype (this is called haploinsufficiency). A disease that is caused by a loss-of-function mutation is Gitelman syndrome and cystic fibrosis. [53]

  4. Gene duplication - Wikipedia

    en.wikipedia.org/wiki/Gene_duplication

    Gene duplication. Gene duplication (or chromosomal duplication or gene amplification) is a major mechanism through which new genetic material is generated during molecular evolution. It can be defined as any duplication of a region of DNA that contains a gene. Gene duplications can arise as products of several types of errors in DNA replication ...

  5. Potocki–Lupski syndrome - Wikipedia

    en.wikipedia.org/wiki/Potocki–Lupski_syndrome

    Potocki–Lupski syndrome (PTLS), also known as dup (17)p11.2p11.2 syndrome, trisomy 17p11.2 or duplication 17p11.2 syndrome, is a contiguous gene syndrome involving the microduplication of band 11.2 on the short arm of human chromosome 17 (17p11.2). [ 1 ] The duplication was first described as a case study in 1996. [ 2 ]

  6. Pelizaeus–Merzbacher disease - Wikipedia

    en.wikipedia.org/wiki/Pelizaeus–Merzbacher_disease

    Pelizaeus–Merzbacher disease is an X-linked neurological disorder that damages oligodendrocytes in the central nervous system. It is caused by mutations in proteolipid protein 1 (PLP1), a major myelin protein. It is characterized by a decrease in the amount of insulating myelin surrounding the nerves (hypomyelination) and belongs to a group ...

  7. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    Duchenne muscular dystrophy. P – Point mutation, or any insertion/deletion entirely inside one gene. D – Deletion of a gene or genes. Dup - Duplication of a gene or genes. C – Whole chromosome extra, missing, or both (see chromosome abnormality) T – Trinucleotide repeat disorders: gene is extended in length.

  8. Chromosome abnormality - Wikipedia

    en.wikipedia.org/wiki/Chromosome_abnormality

    Chromosome abnormality. A chromosomal abnormality, chromosomal anomaly, chromosomal aberration, chromosomal mutation, or chromosomal disorder is a missing, extra, or irregular portion of chromosomal DNA. [1][2] These can occur in the form of numerical abnormalities, where there is an atypical number of chromosomes, or as structural ...

  9. Trinucleotide repeat disorder - Wikipedia

    en.wikipedia.org/wiki/Trinucleotide_repeat_disorder

    In genetics, trinucleotide repeat disorders, a subset of microsatellite expansion diseases (also known as repeat expansion disorders), are a set of over 30 genetic disorders caused by trinucleotide repeat expansion, a kind of mutation in which repeats of three nucleotides (trinucleotide repeats) increase in copy numbers until they cross a threshold above which they cause developmental ...