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Unilateral segmentally arranged basaloid follicular hamartomas with osteoma cutis and hypodontia: a case of Happle-Tinschert syndrome.
Clin Exp Dermatol. 2013 Dec; 38(8):862-5.CE

Abstract

Happle-Tinschert syndrome (HTS) is a rare syndrome characterized by segmentally arranged basaloid follicular hamartomas (BFH) associated with ipsilateral osseous, dental and cerebral abnormalities. Happle and Tinschert first reported this disorder in 2008, and three cases with similar presentations have since been reported. We report another case, that of a 40-year-old man, presenting with the characteristic clinical features of HTS.

Authors+Show Affiliations

Department of Dermatology, Chang Gung Memorial Hospital, Keelung, Taiwan; Chang Gung University College of Medicine, Taoyuan, Taiwan.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

24252078

Citation

Lo, C-S, et al. "Unilateral Segmentally Arranged Basaloid Follicular Hamartomas With Osteoma Cutis and Hypodontia: a Case of Happle-Tinschert Syndrome." Clinical and Experimental Dermatology, vol. 38, no. 8, 2013, pp. 862-5.
Lo CS, Wu YF, Hsiao YW, et al. Unilateral segmentally arranged basaloid follicular hamartomas with osteoma cutis and hypodontia: a case of Happle-Tinschert syndrome. Clin Exp Dermatol. 2013;38(8):862-5.
Lo, C. S., Wu, Y. F., Hsiao, Y. W., Chung, W. H., & Yang, C. H. (2013). Unilateral segmentally arranged basaloid follicular hamartomas with osteoma cutis and hypodontia: a case of Happle-Tinschert syndrome. Clinical and Experimental Dermatology, 38(8), 862-5. https://doi.org/10.1111/ced.12161
Lo CS, et al. Unilateral Segmentally Arranged Basaloid Follicular Hamartomas With Osteoma Cutis and Hypodontia: a Case of Happle-Tinschert Syndrome. Clin Exp Dermatol. 2013;38(8):862-5. PubMed PMID: 24252078.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Unilateral segmentally arranged basaloid follicular hamartomas with osteoma cutis and hypodontia: a case of Happle-Tinschert syndrome. AU - Lo,C-S, AU - Wu,Y-F, AU - Hsiao,Y-W, AU - Chung,W-H, AU - Yang,C-H, PY - 2013/01/31/accepted PY - 2013/11/21/entrez PY - 2013/11/21/pubmed PY - 2014/7/25/medline SP - 862 EP - 5 JF - Clinical and experimental dermatology JO - Clin. Exp. Dermatol. VL - 38 IS - 8 N2 - Happle-Tinschert syndrome (HTS) is a rare syndrome characterized by segmentally arranged basaloid follicular hamartomas (BFH) associated with ipsilateral osseous, dental and cerebral abnormalities. Happle and Tinschert first reported this disorder in 2008, and three cases with similar presentations have since been reported. We report another case, that of a 40-year-old man, presenting with the characteristic clinical features of HTS. SN - 1365-2230 UR - https://www.unboundmedicine.com/medline/citation/24252078/Unilateral_segmentally_arranged_basaloid_follicular_hamartomas_with_osteoma_cutis_and_hypodontia:_a_case_of_Happle_Tinschert_syndrome_ L2 - https://doi.org/10.1111/ced.12161 DB - PRIME DP - Unbound Medicine ER -