Distinctive Skeletal Abnormalities With No Microdeletions or Microduplications on Array-CGH in a Boy With Mohr Syndrome (Oro-Facial-Digital Type II)
| Autor: | Renata Pospischill, Franz Grill, Rudolf Ganger, Ali Al Kaissi |
|---|---|
| Rok vydání: | 2015 |
| Předmět: |
Mohr syndrome
medicine.medical_specialty business.industry Case Report General Medicine Anatomy Synostosis medicine.disease Surgery Hip subluxation Distinctive bony changes medicine Skeletal abnormalities Vertical Talus Radiology Talipes equinovarus business OFD type II Bilateral coxa valga Obtuse mandibular angle |
| Zdroj: | Journal of Clinical Medicine Research |
| ISSN: | 1918-3011 1918-3003 |
| DOI: | 10.14740/jocmr2341w |
| Popis: | We describe a constellation of distinctive skeletal abnormalities in an 8-year-old boy who presented with the full clinical criteria of oro-facial-digital (OFD) type II (Mohr syndrome): bony changes of obtuse mandibular angle, bimanual hexadactyly and unilateral synostosis of the metacarpo-phalanges of 3-4, bilateral coxa valga associated with moderate hip subluxation, over-tubulation of the long bones, vertical talus of the left foot and talipes equinovarus of the right foot respectively. Interestingly, we encountered variable minor malformations in his parents, confirming the autosomal recessive pattern of inheritance. There were no microdeletions or microduplications after performing array-CGH-analysis. We report what might be a constellation of unreported skeletal abnormalities in a child with OFD type II (Mohr syndrome). |
| Databáze: | OpenAIRE |
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