A new syndrome of microtia with mixed type hearing loss, renal agenesis, and multiple skeletal anomalies

We report on a 17‐year‐old man who presented with unreported combination of right sided microtia and preauricular skin tag with conductive hearing loss, unilateral renal agenesis, partial syndactyly of forth and fifth metacarpals, multiple tarsal coalitions, absent toe, and hypoplastic tibia and fib...

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Veröffentlicht in:American journal of medical genetics. Part A 2006-04, Vol.140A (7), p.747-751
Hauptverfasser: Demir, Yavuz, Samli, Hale, Yucel, Aylin, Yilmaz, M. Deniz, Haktanir, Nurten Turhan, Maralcan, Gokhan, Solak, Mustafa
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Sprache:eng
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Zusammenfassung:We report on a 17‐year‐old man who presented with unreported combination of right sided microtia and preauricular skin tag with conductive hearing loss, unilateral renal agenesis, partial syndactyly of forth and fifth metacarpals, multiple tarsal coalitions, absent toe, and hypoplastic tibia and fibula. Radiological and clinical findings did not match with the previously described syndromes with the type of anomalies seen in the case. We propose that this represents a new syndrome. © 2006 Wiley‐Liss, Inc.
ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.31147