Literature DB >> 1472706

A case of atypical Duchenne type muscular dystrophy with fragile X.

N Natori1.   

Abstract

The patient was a 9-year-old boy. He began to walk at the age 1 year and 8 months and began to speak at the age of 2 years, suggesting retarded mental and motor development. A diagnosis of DMD was made when he was 7 years old. On admission, the patient exhibited a peculiar thin and long face, large auricles, narrow palate, malalignment of the teeth, epicanthus, saddle nose, and simian lines in addition to symptoms consistent with DMD. Chromosome analysis showed fragile X at Xq27 at a frequency of 20%. His mother also showed fragile X at the same position. Since the atypical features of this DMD patient are all explained as fragile X syndrome, this case was considered to be a very rare instance of DMD whose clinical pictures were modified by fragile X syndrome.

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Year:  1992        PMID: 1472706     DOI: 10.1007/BF01900718

Source DB:  PubMed          Journal:  Jpn J Hum Genet        ISSN: 0916-8478


  1 in total

1.  Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double Diagnosis.

Authors:  Elisabetta Tabolacci; Maria Grazia Pomponi; Laura Remondini; Roberta Pietrobono; Daniela Orteschi; Veronica Nobile; Cecilia Pucci; Elisa Musto; Marika Pane; Eugenio M Mercuri; Giovanni Neri; Maurizio Genuardi; Pietro Chiurazzi; Marcella Zollino
Journal:  Genes (Basel)       Date:  2021-11-27       Impact factor: 4.096

  1 in total

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