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Oto-palato-digital syndrome type II in two unrelated boys
Authors:Sabine Preis  H. Kemperdick  F. Majewski
Affiliation:Department of Pediatrics, Pediatric Radiology Heinrich Heine Universität, Düsseldorf, Germany;Department of Human Genetics, Pediatric Radiology Heinrich Heine Universität, Düsseldorf, Germany;Department of Diagnostic Radiology, Pediatric Radiology Heinrich Heine Universität, Düsseldorf, Germany;Universitätskinderklinik, Moorenstr. 5, 40225 Düsseldorf, Germany
Abstract:We report on two boys with oto-palato-digital syndrome type II, characterized by growth retardation, bowed long bones, missing or hypoplastic fibulae, sclerosis of the skull base and wavy, irregular clavicles and ribs. The facial appearance is distinctive due to prominent forehead, widely spaced eyes, antimongologid slant of palpebral fissures, flattened nasal bridge and retrogenia. The mother of one patient showed a mild manifestation of oto-palato-digital syndrome type II. Only about 20 cases of this rare X-linked disorder have been reported so far. The similiarities and dissimilarities to oto-palato-digital syndrome type I are discussed.
Keywords:absent/hypoplastic fibula    oto-palato-digital syndrome type II    skeletal dysplasia    X-linked inheritance
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