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Oral-facial-digital syndrome type II (Mohr syndrome): clinical and genetic manifestations.
Sakai N, Nakakita N, Yamazaki Y, Ui K, Uchinuma E. Sakai N, et al. J Craniofac Surg. 2002 Mar;13(2):321-6. doi: 10.1097/00001665-200203000-00028. J Craniofac Surg. 2002. PMID: 12000897
The oral-facial-digital syndromes (OFDS) represent a heterogenous group of disorders characterized by oral malformation, facial anomalies, and digital anomalies. Type II OFDS was reported by Mohr in 1941. Mohr syndrome is an autosomal recessive inherited disease cha …
The oral-facial-digital syndromes (OFDS) represent a heterogenous group of disorders characterized by oral malformation, facial anomalies, a …
Non-syndromic generalised hypotaurodontism in a case of Stage III Grade C periodontitis.
Sethuraman P, Baliah J, Reddy JRC, Umar M. Sethuraman P, et al. BMJ Case Rep. 2023 Apr 28;16(4):e254583. doi: 10.1136/bcr-2023-254583. BMJ Case Rep. 2023. PMID: 37116957
The tooth lack constriction at the cementoenamel junction is mimicking a bull tooth. Taurodontism is usually observed as an isolated tooth aberration. However, it can also be associated with specific syndromes such as Down's syndrome, amelogenesis imperfecta, Klinefelter s …
The tooth lack constriction at the cementoenamel junction is mimicking a bull tooth. Taurodontism is usually observed as an isolated …
Oro-facial-digital syndrome II. Transitional type between the Mohr and the Majewski syndromes: report of two new cases.
Silengo MC, Bell GL, Biagioli M, Franceschini P. Silengo MC, et al. Clin Genet. 1987 May;31(5):331-6. doi: 10.1111/j.1399-0004.1987.tb02817.x. Clin Genet. 1987. PMID: 3608220
Two patients with the oro-facial-digital syndrome II or Mohr syndrome presented laryngeal anomalies and hallucal and postaxial polysyndactyly of the feet. Those rare malformations are typically observed in patients with the Majewski syndrome, a lethal, short …
Two patients with the oro-facial-digital syndrome II or Mohr syndrome presented laryngeal anomalies and hallucal and postaxial …
Mohr syndrome in two siblings.
Gencík A, Gencíkova A. Gencík A, et al. J Genet Hum. 1983 Dec;31(4):307-15. J Genet Hum. 1983. PMID: 6663289
The present study reports on two siblings of different sex, affected with a condition corresponding to Mohr syndrome. Characteristic symptoms such as epicanthic folds, a broad and flattened nasal root, a lobulated and hamartomatous tongue, poly- and syndactyly on bo …
The present study reports on two siblings of different sex, affected with a condition corresponding to Mohr syndrome. Characte …
Oral-facial-digital syndrome with Y-shaped fourth metacarpals and endocardial cushion defect.
Hsieh YC, Hou JW. Hsieh YC, et al. Am J Med Genet. 1999 Sep 17;86(3):278-81. Am J Med Genet. 1999. PMID: 10482880
These clinical manifestations resembled oral-facial-digital syndrome type II (OFDS II, Mohr syndrome) or type VI (Varadi syndrome), associated with an atrioventricular canal. ...In addition to Y-shaped fourth metacarpals, Mohr syndrome plus atrioventri …
These clinical manifestations resembled oral-facial-digital syndrome type II (OFDS II, Mohr syndrome) or type VI (Varadi syndr …
Prenatal diagnosis of Mohr syndrome by ultrasonography.
Iaccarino M, Lonardo F, Giugliano M, Della Bruna MD. Iaccarino M, et al. Prenat Diagn. 1985 Nov-Dec;5(6):415-8. doi: 10.1002/pd.1970050607. Prenat Diagn. 1985. PMID: 3911193
A case of prenatal diagnosis of Mohr syndrome is presented. The ultrasound examination was indicated by the previous birth of an affected brother. The need for genetic counselling is stressed, when polydactyly is observed accidentally at ultrasound examinatio …
A case of prenatal diagnosis of Mohr syndrome is presented. The ultrasound examination was indicated by the previous birth of …