Congenital nonprogressive myopathy with Möbius and Robin sequence—the Carey-Fineman-Ziter syndrome: A confirmatory report
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference12 articles.
1. The Robin sequence as a consequence of malformation, dysplasia, and neuromuscular syndromes
2. New Syndrome? Robin sequence with facial and digital anomalies in two half-brothers by the same mother
3. (1990): “Syndromes of the Head and Neck.” New York: Oxford University Press, p 701.
4. U-shaped palatal defect in the Robin anomalad: Developmental and clinical relevance
5. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: A new autosomal recessive syndrome
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1. Oral Health-Related Quality of Life in Rare Disorders of Congenital Facial Weakness;International Journal of Environmental Research and Public Health;2024-05-13
2. Carey-Fineman-Ziter Syndrome: A MYMK-Related Myopathy Mimicking Brainstem Dysgenesis;Journal of Neuromuscular Diseases;2020-06-02
3. Muscle Involvement and Restricted Disorders;Volpe's Neurology of the Newborn;2018
4. Identification of STAC3 variants in non‐Native American families with overlapping features of Carey–Fineman–Ziter syndrome and Moebius syndrome;American Journal of Medical Genetics Part A;2017-08-04
5. A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome;Nature Communications;2017-07-06
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