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PubMed · 8418656

Apparent Greig cephalopolysyndactyly and sinus node disease.

J P Fryns·P De Waele·L Van der Hauwaert·H Van den Berghe
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Abstract

We present the clinical findings and follow-up data from birth to 10.5 years in a boy with Greig cephalopolysyndactyly who, in addition, presents sinus node disease ("sick sinus syndrome"). The significance of the concurrence of Greig cephalopolysyndactyly syndrome, an autosomal dominant condition mapped at 7p13, and sinus node disease is discussed.

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Abnormalities, MultipleBone and BonesChildChromosome AberrationsChromosome DisordersChromosomes, Human, Pair 7Facial BonesFoot Deformities, CongenitalHand Deformities, CongenitalHeart Defects, CongenitalHumansMaleSinoatrial NodeSkullSyndromeCase ReportsJournal Article

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J P Fryns, P De Waele, L Van der Hauwaert, H Van den Berghe. 1993-01-01. Apparent Greig cephalopolysyndactyly and sinus node disease.. https://doi.org/10.1002/ajmg.1320450111

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