Cover Image

OSTEODISTROFIA HEREDITÁRIA DE ALBRIGHT: UM RELATO DE CASO

O pseudo-hiperparatireoidismo ocorre devido a uma resistência periférica à ação do paratormônio, cursando com hipocalcemia. Quase todos os casos são do tipo IA, correspondente a Síndrome de Osteodistrofia Hereditária de Albright. O presente estudo tem como objetivo relatar o caso de um paci...

Full description

Saved in:

Bibliographic Details
Main Authors:	Bruna Batista de Mesquita de Carvalho (Author), Isadora Benevides da Silva Gondim Nascimento (Author), Cláudia Barros Gonçalves Cunha (Author), Julya de Assis Sousa Morais (Author), Leonardo Meira de Carvalho (Author)
Format:	Book
Published:	Faculdades Nova Esperança, 2020-04-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Osteodistrofia renale vs Osteoporosi
by: S. Mazzaferro, et al.
Published: (2018)

Markers Umorali Nella Osteodistrofia Uremica
by: G. Coen
Published: (1994)

Piropoiquilocitose hereditária no período neonatal - relato de caso
by: Ana Beatriz Teodoro Borges, et al.
Published: (2023)

Síndrome de hiperferritinemia e catarata hereditária: relato de caso
by: Hortência Teixeira de Morais, et al.
Published: (2023)

A case report of Albright syndrome
by: F. Haghighati, et al.
Published: (1994)

Epidermólise bolhosa hereditária
by: Tânia Lopes, et al.
Published: (2014)

Albright hereditary osteodystrophy: dental management case report
by: Stephanie Anagnostopoulos FRIEDRICH, et al.
Published: (2018)

Albright hereditary osteodystrophy: A rare case report
by: Goswami M, et al.
Published: (2009)

Albright's Hereditary Osteodystrophy: A Constellation of Clinical Features
by: L Ambika, et al.
Published: (2010)

McCune-Albright syndrome - A case report with transmission electron microscopy
by: Victor Garcia Neto, et al.
Published: (2022)

Phenotypic testicular abnormalities and pubertal development in boys with McCune-Albright syndrome
by: Tommaso Aversa, et al.
Published: (2018)

TROMBOFILIAS HEREDITARIAS
by: Gustavo Kiekebusch H, et al.
Published: (2003)

Mc cune albright syndrome - Clinicoradiological diagnosis of a rare case
by: Anka Sharma, et al.
Published: (2021)

Severe Neonatal Cholestasis as an Early Presentation of McCune- Albright Syndrome
by: Nicole Coles, et al.
Published: (2019)

Persistent Diabetes Mellitus Postadrenalectomy in Neonatal McCune-Albright Syndrome
by: Mustafa Tosur MD, et al.
Published: (2017)

Dyschromatosis universalis hereditaria
by: Naik Chandra, et al.
Published: (2009)

Lower limbs deformities in patients with McCune-Albright syndrome: Tomography and treatment
by: Ali Al Kaissi, et al.
Published: (2016)

Epidermólisis ampollosa hereditaria: serie de casos
by: S. Guillen-Climent, et al.
Published: (2021)

A novel variant in the GNAS complex locus causes Albright hereditary osteodystrophy with pseudopseudohypoparathyroidism
by: Jeffrey S. Smith, MD, PhD, et al.
Published: (2022)

Dyschromatosis Universalis Hereditaria with Renal Failure
by: Salinee Rojhirunsakool, et al.
Published: (2015)

Dyschromatosis universalis hereditaria with involvement of palms
by: Kikkeri Narayanshetty Naveen, et al.
Published: (2014)

Dyschromatosis Symmetrica Hereditaria of Late Onset?
by: Caroline Balvedi Gaiewski, et al.
Published: (2014)

Telangiectasia hemorrágica hereditária: ácido tranexâmico no tratamento de úlcera plantar Hereditary hemorrhagic telangiectasia: tranexamic acid for plantar ulcer
by: Gabriella Corrêa de Albuquerque, et al.
Published: (2005)

Cenário das políticas públicas para hemocromatose hereditária no Brasil
by: Cristiane da Silva Rodrigues de Araújo, et al.
Published: (2023)

A non-classic form of McCune Albright syndrome with different presentations and review of the literatures
by: Ali Reza Navabazam, et al.
Published: (2021)

McCune-Albright Syndrome With Unremitting Hyperthyroidism at Early Age: Management Perspective for Early Thyroidectomy
by: Nadia Merchant MD, et al.
Published: (2019)

MANEJO DE LA EMBARAZADA CON TROMBOFILIA HEREDITARIA
by: Jorge Hasbún H., et al.
Published: (2003)

Displasia ectodérmica hereditária e hipótese de Lyon
by: Camila Helena Machado da Costa, et al.

Telangiectasia hemorrágica hereditaria Hereditary hemorrhagic telangiectasia
by: Raymundo Rafael Fernández Díaz, et al.
Published: (2009)

Osteocondromatosis múltiple hereditaria en una familia
by: Jesús Santos-Guzmán, et al.
Published: (2016)

Craniofacial fibrous dysplasia associated with McCune-Albright syndrome: challenges in diagnosis and treatment: case reports
by: Theodora Miti Kabali, et al.
Published: (2019)

Neonatal cholestasis as the onset symptom of McCune-Albright syndrome: case reports and a literature review
by: Weiyuan Fang, et al.
Published: (2023)

Pituitary mammosomatotroph tumor with folliculo-stellate and mucin cells in a child with McCune Albright syndrome
by: Sadeem Al-Subaie, et al.
Published: (2019)

Telangiectasia hemorrágica hereditaria. A propósito de dos casos.
by: Mildrey Jiménez López, et al.
Published: (2009)

Uso de bevacizumab en la telangiectasia hemorrágica hereditaria: reporte de caso
by: Darío González Viñas, et al.
Published: (2022)

Relato de experiência e investigação de aplicação de um personagem fictício como método na aprendizagem de Anatomia Humana
by: Emília Cristina Benevides de Freitas, et al.
Published: (2022)

Relato de experiência e investigação de aplicação de um personagem fictício como método na aprendizagem de Anatomia Humana
by: Emília Cristina Benevides de Freitas, et al.
Published: (2022)

Dyschromatosis universalis hereditaria with keratoacanthoma: a rare presentation
by: Veena Thimmappa, et al.
Published: (2022)

Dyschromatosis universalis hereditaria with keratoacanthoma: a rare presentation
by: Veena
Published: (2022)

Dyschromatosis universalis hereditaria: A rare case report
by: Esha Bisne, et al.
Published: (2013)