Berk–Tabatznik syndrome
 | This article needs more links to other articles to help integrate it into the encyclopedia. (July 2016) |
Berk–Tabatznik syndrome is a condition with an unknown cause that shows symptoms of short stature, congenital optic atrophy and brachytelephalangy. This condition is extremely rare with only two cases being found.[1]
See also
References
- ^ Bissonnette, Bruno; Luginbuehl, Igor; Dalens, Bernard J., eds. (2006). "Berk–Tabatznik Syndrome". Syndromes: rapid recognition and perioperative implications. New York: McGraw-Hill. p. 94. ISBN 978-0-07-135455-4.
{{cite book}}: External link in|chapterurl=|chapterurl=ignored (|chapter-url=suggested) (help)
Further reading
- Hartwell, EA; Robinson, LK; Robinson, LH; Aceves, J; Reynolds, James F. (1988). "Congenital optic atrophy and brachytelephalangy: the Berk–Tabatznik syndrome". American Journal of Medical Genetics. 29 (2): 383–9. doi:10.1002/ajmg.1320290220. PMID 3128111.
 | This article about a congenital malformation is a stub. You can help Wikipedia by expanding it. |