Long-term dental management of a patient with features of Schöpf-Schulz-Passarge syndrome-Reference-Cited by-同舟云学术

Long-term dental management of a patient with features of Schöpf-Schulz-Passarge syndrome

Published:2017-06-09 Issue:4 Volume:37 Page:204-208
ISSN:0275-1879
Container-title:Special Care in Dentistry
language:en
Short-container-title:Spec Care Dentist

Author:

Manchanda Nandika¹,Anthonappa Robert²^ORCID,Al-Mulla Hessa³,King Nigel⁴

Affiliation:

1. Paediatric Dental Registrar, School of Dentistry; The University of Western Australia; Australia

2. Discipline Lead and Program Convenor, Paediatric Dentistry, School of Dentistry; The University of Western Australia; Australia

3. Paediatric Dentistry; Hamad Medical Corporation; Qatar

4. Professor, Paediatric Dentistry, School of Dentistry; The University of Western Australia; Australia

Publisher

Wiley

Subject

General Dentistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/scd.12228/fullpdf

Reference34 articles.

1. Syndrome of cystic eyelids, palmo-plantar keratosis, hypodontia and hypotrichosis as a possible autosomal recessive trait;Schöpf;Birth Defects Orig Artic Ser,1971

2. Schöpf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations;Castori;Acta Derm Venereol,2008

3. A case of Schöpf-Schulz-Passarge syndrome;Hampton;Clin Exp Dermatol,2005

4. Eccrine syringofibroadenoma: multiple lesions representing a new cutaneous marker of the Schöpf syndrome, and solitary nonhereditary tumors;Starink;J Am Acad Dermatol,1997

5. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes;Bohring;Am J Hum Genet,2009

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