Cargando…

Periodontal profile and radiographic characterization of the jaws in a patient with autosomal dominant osteopetrosis

Osteopetrosis (OP) comprehends a rare group of conditions, presenting on radiographs increased bone density, deriving from irregularities in osteoclast differentiation or function. In the autosomal dominant osteopetrosis (ADO), some patients stay asymptomatic for some time, or only develop mild symp...

Descripción completa

Detalles Bibliográficos
Autores principales:	da Silva Barbirato, Davi, Fogacci, Mariana Fampa, Arruda, Mariana, Rodrigues, Monique Oliveira, Neto, Leonardo Vieira
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Bioscientifica Ltd 2017
Materias:	Insight into Disease Pathogenesis or Mechanism of Therapy
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409937/ https://www.ncbi.nlm.nih.gov/pubmed/28469925 http://dx.doi.org/10.1530/EDM-16-0106

Ejemplares similares

Brown tumor of the jaw after pregnancy and lactation in a MEN1 patient
por: Casteràs, Anna, et al.
Publicado: (2016)

Bilateral pheochromocytoma after kidney transplantation in neurofibromatosis type 1
por: de Miguel, Valeria, et al.
Publicado: (2019)

A clinically novel AIP mutation in a patient with a very large, apparently sporadic somatotrope adenoma
por: Salvatori, Roberto, et al.
Publicado: (2014)

The dilemma of the gender assignment in a Portuguese adolescent with disorder of sex development due to 17β-hydroxysteroid-dehydrogenase type 3 enzyme deficiency
por: Costa, Carla, et al.
Publicado: (2014)

Bilateral adrenal gland haemorrhage: an unusual cause
por: Gowda, Durgesh, et al.
Publicado: (2014)

Pituitary metastases from papillary carcinoma of thyroid: a case report and literature review
por: Chikani, Viral, et al.
Publicado: (2013)

Vanishing hypercalciuric kidney stones after treating underlying acromegaly
por: van der Valk, Eline, et al.
Publicado: (2013)

First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene
por: Casey, R, et al.
Publicado: (2013)

Identification of a novel heterozygous mutation in exon 50 of the COL1A1 gene causing osteogenesis imperfecta
por: Aftab, S A S, et al.
Publicado: (2013)

Radioiodine treatment of differentiated thyroid cancer despite history of ‘iodine allergy’
por: Puchalski, Adam R, et al.
Publicado: (2014)

Tumor-induced osteomalacia due to a recurrent mesenchymal tumor overexpressing several growth factor receptors
por: Yavropoulou, Maria P, et al.
Publicado: (2015)

Autoimmune alternating hyper- and hypo-thyroidism: a rare condition in pediatrics
por: Martins, Luísa Correia, et al.
Publicado: (2016)

Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene
por: Nobel, Yael R, et al.
Publicado: (2016)

Successful fertility treatment with gonadotrophin therapy for male hypogonadotrophic hypogonadism
por: Rajkanna, J, et al.
Publicado: (2016)

Asymptomatic Paget's disease of bone in a 62-year-old Nigerian man: three years post-alendronate therapy
por: Aransiola, Clement Olukayode, et al.
Publicado: (2016)

Heterogeneity of glucagonomas due to differential processing of proglucagon-derived peptides
por: Challis, Benjamin G, et al.
Publicado: (2015)

Xanthogranulomatous hypophysitis: a rare and often mistaken pituitary lesion
por: Gopal-Kothandapani, Jaya Sujatha, et al.
Publicado: (2015)

Pancreas-protective effect of rituximab for acute-onset type 1 diabetes in the honeymoon period: a case report
por: Kurozumi, Akira, et al.
Publicado: (2016)

Lipoid congenital adrenal hyperplasia due to STAR mutations in a Caucasian patient
por: Kaur, Jasmeet, et al.
Publicado: (2016)

A novel immunopathological association of IgG4-RD and vasculitis with Hashimoto's thyroiditis
por: Minamino, Hiroto, et al.
Publicado: (2016)

Gonadotropin-releasing hormone agonist-induced pituitary apoplexy
por: Keane, Fergus, et al.
Publicado: (2016)

Thyroid antibody-negative euthyroid Graves’ ophthalmopathy
por: Tabasum, Arshiya, et al.
Publicado: (2016)

Adrenal cancer in neurofibromatosis type 1: case report and DNA analysis
por: Menon, Ravi Kumar, et al.
Publicado: (2014)

Impact of a novel 14 bp MEN1 deletion in a patient with hyperparathyroidism and gastrinoma
por: Birla, Shweta, et al.
Publicado: (2015)

Transient diabetes insipidus in pregnancy
por: Marques, Pedro, et al.
Publicado: (2015)

Cushing's storm secondary to a rare case of ectopic ACTH secreting metastatic breast cancer
por: Bucciarelli, Maura, et al.
Publicado: (2015)

Resistant hypertension with adrenal nodule: are we removing the right gland?
por: Das, Gautam, et al.
Publicado: (2015)

Follicular thyroid carcinoma with NRAS Q61K and GNAS R201H mutations that had a good (131)I treatment response
por: Lu, Jin-Ying, et al.
Publicado: (2016)

Management of metastatic thyroid cancer in pregnancy: risk and uncertainty
por: Rowe, Christopher W, et al.
Publicado: (2016)

Flying under the radar: treatment of refractory hyperglycemia
por: Kandel, S M, et al.
Publicado: (2016)

Insulin Autoimmune Syndrome: a rare cause of postprandial hypoglycemia
por: Sahni, Pooja, et al.
Publicado: (2016)

Novel SCC mutation in a patient of Mexican descent with sex reversal, salt-losing crisis and adrenal failure
por: Kaur, Jasmeet, et al.
Publicado: (2016)

Refractory hypoglycemia in a patient with functional adrenal cortical carcinoma
por: Marchetti, Katia Regina, et al.
Publicado: (2016)

Autoimmune polyendocrinopathy and hypophysitis after Puumala hantavirus infection
por: Tarvainen, Marlene, et al.
Publicado: (2016)

Growth of a progesterone receptor-positive meningioma in a female patient with congenital adrenal hyperplasia
por: O’Shea, T, et al.
Publicado: (2016)

Pancreatic α-cell hyperplasia and hyperglucagonemia due to a glucagon receptor splice mutation
por: Larger, Etienne, et al.
Publicado: (2016)

Clinical challenges in the management of isolated GH deficiency type IA in adulthood
por: Casteràs, Anna, et al.
Publicado: (2014)

Cured primary hyperparathyroidism after fine-needle aspiration biopsy-induced parathyroid disappearance
por: Kara, Elda, et al.
Publicado: (2017)

A rare cause of primary adrenal insufficiency due to a homozygous Arg188Cys mutation in the STAR gene
por: Burget, Lukas, et al.
Publicado: (2018)

Growth trajectory and pubertal tempo from birth till final height in a girl with Wolf-Hirschhorn syndrome
por: Siew, Jia Xuan, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_ktemac6abu4e3t1oam9ressd23