Dental abnormalities in rare genetic bone diseases: Literature review

Pycnodysostosis in children and adults

(2023) Jannie Dahl Hald et al.   BONE

The patient clinical journey and socioeconomic impact of osteogenesis imperfecta: a systematic scoping review

(2023) Maria Rapoport et al.   Orphanet Journal of Rare Diseases

Drug-induced osteopetrosis

(2023) Michael P. Whyte et al.   BONE

Oral health-related quality of life in patients with oligodontia: A FACE-Q assessment

(2023) M. Aarts et al.   JOURNAL OF DENTISTRY

The mineralization regulator ANKH mediates cellular efflux of ATP , not pyrophosphate

(2022) Flora Szeri et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Nonsyndromic supernumerary teeth in patients in National Taiwan University Children's hospital

(2022) Feng-Chou Cheng et al.   Journal of Dental Sciences

Efficacy of three surgical methods for gingivectomy of permanent anterior teeth with delayed tooth eruption in children

(2022) Dan Xu et al.   Head & Face Medicine

Prepubertal Periodontitis in a Patient with Combined Classical and Periodontal Ehlers–Danlos Syndrome

(2021) Friedrich Stock et al.   Biomolecules

Missing and unerupted teeth in osteogenesis imperfecta

(2021) Doaa Taqi et al.   BONE

Characteristic dental pattern with hypodontia and short roots in Fraser syndrome

(2020) Felix Kunz et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Malocclusion traits and oral health–related quality of life in children with osteogenesis imperfecta

(2020) Mohammadamin Najirad et al.   JOURNAL OF THE AMERICAN DENTAL ASSOCIATION

The membrane protein ANKH is crucial for bone mechanical performance by mediating cellular export of citrate and ATP

(2020) Flora Szeri et al.   PLoS Genetics

Oral Health‐related Quality of Life in X‐linked Hypophosphatemia and Osteogenesis Imperfecta

(2020) H. Gjørup et al.   JOURNAL OF ORAL REHABILITATION

Oral symptoms and oral health-related quality of life of individuals with x-linked hypophosphatemia

(2019) Marcel Hanisch et al.   Head & Face Medicine

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement

(2019) I. Harting et al.   AMERICAN JOURNAL OF NEURORADIOLOGY

Self-Assessment of Oral Health-Related Quality of Life in People with Ectodermal Dysplasia in Germany

(2019) Marcel Hanisch et al.   International Journal of Environmental Research and Public Health

Hypomineralisation or hypoplasia?

(2019) Ayesha Patel et al.   BRITISH DENTAL JOURNAL

Phenotypic Properties of Collagen in Dentinogenesis Imperfecta Associated with Osteogenesis Imperfecta

(2019) S Ibrahim et al.   International Journal of Nanomedicine

Oral health-related quality of life in Loeys-Dietz syndrome, a rare connective tissue disorder: an observational cohort study

(2019) Quynh C. Nguyen et al.   Orphanet Journal of Rare Diseases

Dental anomalies and orthodontic characteristics in patients with pseudohypoparathyroidism

(2019) Jane Hejlesen et al.   BMC Oral Health

National clinical guidelines for the management of unerupted maxillary incisors in children

(2018) J. Seehra et al.   BRITISH DENTAL JOURNAL

Genetics of Osteopetrosis

(2018) Eleonora Palagano et al.   Current Osteoporosis Reports

RUNX2 mutation impairs osteogenic differentiation of dental follicle cells

(2018) Yang Liu et al.   ARCHIVES OF ORAL BIOLOGY

Main genetic entities associated with supernumerary teeth

(2018)   Archivos Argentinos de Pediatria

Oral health-related quality of life in children and adolescents with osteogenesis imperfecta: cross-sectional study

(2018) Mohammadamin Najirad et al.   Orphanet Journal of Rare Diseases

Early Rehabilitation of Incisors with Dentinogenesis Imperfecta Type II – Case Report

(2017) Ana Paula CA Beltrame et al.   Journal of Clinical Pediatric Dentistry

Prevalence of dental developmental anomalies of permanent teeth in children and their influence on esthetics

(2017) Anita Fekonja   Journal of Esthetic and Restorative Dentistry

Distribution of Cathepsin K in Late Stage of Tooth Germ Development and Its Function in Degrading Enamel Matrix Proteins in Mouse

(2017) Tao Jiang et al.   PLoS One

Failure of tooth eruption and brachydactyly in pseudohypoparathyroidism are not related to plasma parathyroid hormone-related protein levels

(2016) Mariana Tenorio Antunes Reis et al.   BONE

Oculodentodigital dysplasia

(2016) DharmilC Doshi et al.   INDIAN JOURNAL OF OPHTHALMOLOGY

Risks and Benefits of Bisphosphonate Therapies

(2015) Carlen Reyes et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

Enamel Hypomineralization and Structural Defects in Amelotin-deficient Mice

(2015) Y. Nakayama et al.   JOURNAL OF DENTAL RESEARCH

Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta

(2014) James A. Poulter et al.   HUMAN MOLECULAR GENETICS

Diagnosis and Management of Osteonecrosis of the Jaw: A Systematic Review and International Consensus

(2014) Aliya A Khan et al.   JOURNAL OF BONE AND MINERAL RESEARCH

The Molecular Basis of Hereditary Enamel Defects in Humans

(2014) J.T. Wright et al.   JOURNAL OF DENTAL RESEARCH

Dental Anomalies Associated with Craniometaphyseal Dysplasia

(2014) I.-P. Chen et al.   JOURNAL OF DENTAL RESEARCH

Dentinogenesis imperfecta type II: Ultrastructure of teeth in sagittal sections

(2013) Aneta Wieczorek et al.   FOLIA HISTOCHEMICA ET CYTOBIOLOGICA

Homozygous and Compound Heterozygous MMP20 Mutations in Amelogenesis Imperfecta

(2013) B. Gasse et al.   JOURNAL OF DENTAL RESEARCH

Osteopetrosis: genetics, treatment and new insights into osteoclast function

(2013) Cristina Sobacchi et al.   Nature Reviews Endocrinology

Oral manifestations of patients with Kenny–Caffey Syndrome

(2012) Youssra Moussaid et al.   European Journal of Medical Genetics

Dental Abnormalities in a Mouse Model for Craniometaphyseal Dysplasia

(2012) E.H. Dutra et al.   JOURNAL OF DENTAL RESEARCH

Cherubism: best clinical practice

(2012) Maria E Papadaki et al.   Orphanet Journal of Rare Diseases

Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome

(2011) Yigal Dror et al.   Annals of the New York Academy of Sciences

Craniofacial and intraoral phenotype of Robinow syndrome forms

(2011) S Beiraghi et al.   CLINICAL GENETICS

Wnt5a regulates growth, patterning, and odontoblast differentiation of developing mouse tooth

(2011) Minkui Lin et al.   DEVELOPMENTAL DYNAMICS

The Paradox of Better Subjective Oral Health in Older Age

(2011) G.D. Slade et al.   JOURNAL OF DENTAL RESEARCH

The incidence of canine transmigration and tooth impaction in a Turkish subpopulation

(2010) A. M. Aktan et al.   EUROPEAN JOURNAL OF ORTHODONTICS

Decreased levels of Cx43 gap junctions result in ameloblast dysregulation and enamel hypoplasia inGja1Jrt/+mice

(2010) K. Toth et al.   JOURNAL OF CELLULAR PHYSIOLOGY

Dental management of oculodentodigital dysplasia: a case report

(2010) Naser A. Aminabadi et al.   Journal of Oral Science

Non-syndromic concomitant hypodontia and supernumerary teeth in an orthodontic population

(2009) M. Varela et al.   EUROPEAN JOURNAL OF ORTHODONTICS

PHEX analysis in 118 pedigrees reveals new genetic clues in hypophosphatemic rickets

(2009) Céline Gaucher et al.   HUMAN GENETICS

GJA1mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

(2009) William A. Paznekas et al.   HUMAN MUTATION

Genetic basis of tooth agenesis

(2009) Pekka Nieminen   JOURNAL OF EXPERIMENTAL ZOOLOGY PART B-MOLECULAR AND DEVELOPMENTAL EVOLUTION

Osteopetrosis

(2009) Zornitza Stark et al.   Orphanet Journal of Rare Diseases

Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis

(2008) Dong Han et al.   European Journal of Medical Genetics

Why rare diseases are an important medical and social issue

(2008) Arrigo Schieppati et al.   LANCET

Tooth abnormalities and soft tissue alterations in patients with G/BBB syndrome

(2008) G da Silva Dalben et al.   ORAL DISEASES