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Ackerman syndrome is inherited in an autosomal recessive manner
Ackerman syndrome or interstitial granulomatous dermatitis 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.
It was described by James L. Ackerman, A. Leon Ackerman, and A. Bernard Ackerman.
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Treatment
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References
Ackerman JL, Ackerman AL, Ackerman AB (1973). "Taurodont, pyramidal and fused molar roots associated with other anomalies in a kindred". Am. J. Phys. Anthropol. 38 (3): 681–94. doi:10.1002/ajpa.1330380305. PMID4349385.
Busquets-Pérez N, Narvaez J, Valverde-García J (2006). "Interstitial granulomatous dermatitis with arthritis (Ackerman syndrome)". J. Rheumatol. 33 (6): 1207–9. PMID16755676.
Kroesen S, Itin PH, Hasler P (2003). "Arthritis and interstitial granulomatous dermatitis (Ackerman syndrome) with pulmonary silicosis". Semin. Arthritis Rheum. 32 (5): 334–40. doi:10.1053/sarh.2003.50016. PMID12701044.
