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A typical Hallermann-Streiff syndrome in a 3 year old child.
J Clin Pediatr Dent. 1995 Fall; 20(1):63-8.JC

Abstract

Hallermann Streiff syndrome is a rare congenital disorder characterized by dyscephaly, dental anomalies, proportionate nanism, hypotrichosis, cutaneous atrophy limited to the head, bilateral congenital cataracts and bilateral microphthalmia. Despite the marked craniofacial characteristics and oral findings, a relative lack of reports in the dental literature has been noted. In this article, a review of the literature regarding the general clinical features and differential diagnosis is presented. A case of a 3-year-old female is reported with special consideration on the management of her dental problems under general anesthesia. The anesthetic risks of such a procedure as well as the prognosis of her dental development are being discussed.

Authors+Show Affiliations

Department of Pediatric Dentistry, University of Athens, Greece.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article
Review

Language

eng

PubMed ID

8634201

Citation

Vadiakas, G, et al. "A Typical Hallermann-Streiff Syndrome in a 3 Year Old Child." The Journal of Clinical Pediatric Dentistry, vol. 20, no. 1, 1995, pp. 63-8.
Vadiakas G, Oulis C, Tsianos E, et al. A typical Hallermann-Streiff syndrome in a 3 year old child. J Clin Pediatr Dent. 1995;20(1):63-8.
Vadiakas, G., Oulis, C., Tsianos, E., & Mavridou, S. (1995). A typical Hallermann-Streiff syndrome in a 3 year old child. The Journal of Clinical Pediatric Dentistry, 20(1), 63-8.
Vadiakas G, et al. A Typical Hallermann-Streiff Syndrome in a 3 Year Old Child. J Clin Pediatr Dent. 1995;20(1):63-8. PubMed PMID: 8634201.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A typical Hallermann-Streiff syndrome in a 3 year old child. AU - Vadiakas,G, AU - Oulis,C, AU - Tsianos,E, AU - Mavridou,S, PY - 1995/1/1/pubmed PY - 1995/1/1/medline PY - 1995/1/1/entrez SP - 63 EP - 8 JF - The Journal of clinical pediatric dentistry JO - J Clin Pediatr Dent VL - 20 IS - 1 N2 - Hallermann Streiff syndrome is a rare congenital disorder characterized by dyscephaly, dental anomalies, proportionate nanism, hypotrichosis, cutaneous atrophy limited to the head, bilateral congenital cataracts and bilateral microphthalmia. Despite the marked craniofacial characteristics and oral findings, a relative lack of reports in the dental literature has been noted. In this article, a review of the literature regarding the general clinical features and differential diagnosis is presented. A case of a 3-year-old female is reported with special consideration on the management of her dental problems under general anesthesia. The anesthetic risks of such a procedure as well as the prognosis of her dental development are being discussed. SN - 1053-4628 UR - https://www.unboundmedicine.com/medline/citation/8634201/A_typical_Hallermann_Streiff_syndrome_in_a_3_year_old_child_ L2 - http://www.diseaseinfosearch.org/result/3225 DB - PRIME DP - Unbound Medicine ER -