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Catel Manzke Syndrome - National Organization for …

    https://www.rarediseases.org/rare-diseases/catel-manzke-syndrome/
    Catel-Manzke syndrome was first described in the medical literature in 1961 by Dr. Catel and later further evaluated by Dr. Manzke in 1966. The disorder was originally referred to as a palatodigital syndrome, but because cleft palate does not always occur, …

Catel Manzke syndrome - About the Disease - Genetic …

    https://rarediseases.info.nih.gov/diseases/28/catel-manzke-syndrome/
    Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with …

Catel–Manzke syndrome - Wikipedia

    https://en.wikipedia.org/wiki/Catel%E2%80%93Manzke_syndrome

    Orphanet: Catel Manzke syndrome

      https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=1388
      Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with Pierre Robin sequence …

    Catel-Manzke syndrome - NIH Genetic Testing Registry …

      https://www.ncbi.nlm.nih.gov/gtr/conditions/C1844887/
      Catel-Manzke syndrome is characterized by the Pierre Robin anomaly, which comprises cleft palate, glossoptosis, and micrognathia, and a unique form of bilateral …

    Catel-Manzke Syndrome - DoveMed

      https://www.dovemed.com/diseases-conditions/catel-manzke-syndrome/
      Catel-Manzke Syndrome is a rare congenital disorder that has been observed in less than 35 individuals (so far) The presentation of symptoms may occur at birth …

    Catel-Manzke syndrome without Manzke dysostosis

      https://pubmed.ncbi.nlm.nih.gov/31833187/
      Approximately 40 patients with Catel-Manzke have been reported, all with the pathognomonic bilateral or unilateral hyperphalangy caused by an accessory bone …

    Catel-Manzke syndrome | Radiology Reference Article

      https://radiopaedia.org/articles/catel-manzke-syndrome
      Catel-Manzke syndrome is a digitopalatal syndrome initially described in 1961. Inheritance pattern is unknown. Radiographic findings include micronagthia and …

    Catel-Manzke syndrome: two new patients and a critical …

      https://pubmed.ncbi.nlm.nih.gov/18501694/
      Classified into four groups there are now (1) 23 reported cases of the typical, (2) six cases of the extended Catel-Manzke syndrome showing more than two accessory bones in …

    Catel Manzke syndrome - National Organization for Rare …

      https://rarediseases.org/gard-rare-disease/catel-manzke-syndrome/
      NIH GARD Information: Catel Manzke syndrome This information is provided by the National Institutes of Health (NIH) Genetic and Rare Diseases Information Center …



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