Ackerman syndrome
From Infogalactic: the planetary knowledge core
Ackerman syndrome | |
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Classification and external resources | |
Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
OMIM | 200970 |
Patient UK | Ackerman syndrome |
Ackerman syndrome is a familial syndrome of fused molar roots with a single canal (taurodontism), hypotrichosis, full upper lip without a cupid’s bow, thickened and wide philtrum, and occasional juvenile glaucoma.[1] It was described by James L. Ackerman, A. Leon Ackerman, and A. Bernard Ackerman [2]
It can also refer to interstitial granulomatous dermatitis.[3][4]
References
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External links
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