• Thumbnail for Cri du chat syndrome
    Cri du chat syndrome is a rare genetic disorder due to a partial chromosome deletion on chromosome 5. Its name is a French term ("cat-cry" or "call of...
    10 KB (1,147 words) - 05:10, 12 December 2023
  • deletion syndromes include 5p-Deletion (cri du chat syndrome), 4p-Deletion (Wolf–Hirschhorn syndrome), Prader–Willi syndrome, and Angelman syndrome. The chromosomal...
    9 KB (1,128 words) - 00:28, 24 May 2023
  • Thumbnail for Palpebral fissure
    whereas Marfan syndrome can cause a downslant. An increase in vertical height can be seen in genetic disorders such as cri-du-chat syndrome. The fissure...
    3 KB (282 words) - 16:00, 18 May 2024
  • "History and Prevalence of Cri du Chat Syndrome". findresources. Retrieved 15 June 2020. "OMIM Entry - # 123450 - Cri-Du-Chat Syndrome". "Distal Myopathies...
    42 KB (969 words) - 16:02, 3 April 2024
  • Thumbnail for Hypertelorism
    neurofibromatosis, LEOPARD syndrome, Crouzon syndrome, Wolf–Hirschhorn syndrome, Andersen–Tawil syndrome, Waardenburg syndrome and cri du chat syndrome, along with piebaldism...
    10 KB (1,104 words) - 06:59, 15 September 2023
  • syndrome Turner syndrome Noonan syndrome Patau syndrome DiGeorge syndrome Cri du chat syndrome Edwards syndrome Fragile X syndrome Okamoto syndrome It...
    4 KB (283 words) - 00:15, 31 January 2023
  • Thumbnail for Jérôme Lejeune
    abnormalities, most especially the link between Down Syndrome and trisomy-21 and cri du chat syndrome, amongst several others, and for his subsequent strong...
    22 KB (2,447 words) - 02:16, 28 May 2024
  • Thumbnail for Down syndrome
    Down syndrome or Down's syndrome, also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome...
    150 KB (15,021 words) - 03:41, 1 June 2024
  • commonly involve de novo mutations include cri-du-chat syndrome, 1p36 deletion syndrome, genetic cancer syndromes, and certain forms of autism, among others...
    7 KB (775 words) - 05:46, 28 March 2024
  • Thumbnail for Turner syndrome
    Turner syndrome (TS), also known as 45,X, or 45,X0, is a genetic disorder in which a person's cells have only one X chromosome or are partially missing...
    78 KB (9,161 words) - 08:16, 21 May 2024