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Klin Padiatr 2015; 227(05): 296-298
DOI: 10.1055/s-0035-1555921
Pictorial Essay
© Georg Thieme Verlag KG Stuttgart · New York

Gyrate Atrophy in 2 Siblings – Ophthalmological Findings and A New Mutation

Gyratatrophie im Kindesalter
M. Michel
1   Department for Pediatrics, Pediatrics I, Medical University Innsbruck, Innsbruck, Austria
,
G. Blatsios
2   Deparment for Ophthalmology, Medical University Innsbruck, Innsbruck, Germany
,
S. Scholl-Bürgi
1   Department for Pediatrics, Pediatrics I, Medical University Innsbruck, Innsbruck, Austria
,
A. Entenmann
1   Department for Pediatrics, Pediatrics I, Medical University Innsbruck, Innsbruck, Austria
,
A. Wernstedt
3   Department for Clinical Genetics, Medical University Innsbruck, Innsbruck, Austria
,
A. Zschocke
1   Department for Pediatrics, Pediatrics I, Medical University Innsbruck, Innsbruck, Austria
,
K. Pichler
1   Department for Pediatrics, Pediatrics I, Medical University Innsbruck, Innsbruck, Austria
,
A. Höller
1   Department for Pediatrics, Pediatrics I, Medical University Innsbruck, Innsbruck, Austria
,
D. Karall
1   Department for Pediatrics, Pediatrics I, Medical University Innsbruck, Innsbruck, Austria
› Author Affiliations
Further Information

Publication History

Publication Date:
10 August 2015 (online)

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Key words

Gyrate atrophy - Ornithine - Metabolic disease - Systemic disease

Schlüsselwörter

Gyratatrophie - Ornithin - Stoffwechselerkrankung - Systemische Erkrankung
 

  • References

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