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  2. 22q13 deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/22q13_deletion_syndrome

    22q13 deletion syndrome, known as Phelan–McDermid syndrome (PMS), is a genetic disorder caused by deletions or rearrangements on the q terminal end (long arm) of chromosome 22. Any abnormal genetic variation in the q13 region that presents with significant manifestations ( phenotype ) typical of a terminal deletion may be diagnosed as 22q13 ...

  3. Trisomy 22 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_22

    22q13 deletion syndrome (Phelan–McDermid syndrome) [4] is a condition caused by the deletion of the tip of the q arm on chromosome 22. Most individuals with this disorder experience cognitive delays, low muscle tone, and sleeping, eating, and behavioural issues.

  4. Phelan-McDermid syndrome - Wikipedia

    en.wikipedia.org/?title=Phelan-McDermid_syndrome&...

    This page was last edited on 22 July 2006, at 23:58 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may ...

  5. Ring chromosome 22 - Wikipedia

    en.wikipedia.org/wiki/Ring_chromosome_22

    Significant overlap exists between the phenotype of ring chromosome 22 and that of Phelan-McDermid syndrome, another chromosome 22 deletion syndrome. This is ascribed to a shared deletion of the SHANK3 gene at 22q13.3.

  6. Chromosome 22 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_22

    The loss of one particular gene, TBX1, is thought to be responsible for many of the characteristic features of 22q11.2 deletion syndrome, such as heart defects, an opening in the roof of the mouth (a cleft palate), distinctive facial features, and low calcium levels. A loss of this gene does not appear to cause learning disabilities, however.

  7. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    Phelan-McDermid syndrome: 22q13 D Phenylketonuria: PAH: recessive 1:12,000 Pipecolic acidemia: AASDHPPT: recessive Pitt–Hopkins syndrome: TCF4 (18) dominant, de novo 1:11,000-41,000 Polycystic kidney disease: PKD1 (16) or PKD2 (4) P Polycystic ovary syndrome (PCOS) Porphyria: 1-100:50,000 Prader–Willi syndrome: 15: paternal imprinting 1: ...

  8. Asymmetric crying facies - Wikipedia

    en.wikipedia.org/wiki/Asymmetric_crying_facies

    Asymmetric crying facies (ACF), also called partial unilateral facial paresis and hypoplasia of depressor angula oris muscle, [1] is a minor congenital anomaly caused by agenesis or hypoplasia of the depressor anguli oris muscle, one of the muscles that control the movements of the lower lip. This unilateral facial weakness is first noticed ...

  9. Facies (medical) - Wikipedia

    en.wikipedia.org/wiki/Facies_(medical)

    Bovine facies (or cow face) – craniofacial dysostosis or Crouzon syndrome; Marshall halls facies – hydrocephalus; Frog face – intranasal disease; Coarse facies – many inborn errors of metabolism; Adenoid facies – developmental facial traits caused by adenoid hypertrophy, nasal airway obstruction and mouthbreathing; really a form of ...