Abstract
We report on a boy with unique somatic and skeletal manifestations. The syndrome consists of branchial and auricular fistulae, abnormal face, and skeletal abnormalities including foramina parietalia permagna.
MeSH terms
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Abnormalities, Multiple* / diagnostic imaging
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Ear / abnormalities
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Face / abnormalities
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Genitalia, Male / abnormalities
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Hand Deformities, Congenital / diagnostic imaging
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Humans
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Infant, Newborn
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Karyotyping
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Male
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Mouth Abnormalities
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Parietal Bone / abnormalities*
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Parietal Bone / diagnostic imaging
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Phenotype
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Radiography
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Scoliosis / diagnostic imaging
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Syndrome
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Toes / abnormalities