Cargando…

Bariatric surgery in an obese patient with Albright hereditary osteodystrophy: a case report

INTRODUCTION: We report for the first time the case of a patient with Albright hereditary osteodystrophy and pseudopseudohypoparathyroidism who underwent a Roux-en-Y gastric bypass. CASE PRESENTATION: A 26-year-old obese Caucasian woman with Albright hereditary osteodystrophy with pseudopseudohypopa...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ferrario, Chiara, Gastaldi, Giacomo, Portmann, Luc, Giusti, Vittorio
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3651286/ https://www.ncbi.nlm.nih.gov/pubmed/23617958 http://dx.doi.org/10.1186/1752-1947-7-111

Ejemplares similares

Bilateral Simultaneous Disc Edema and Cataract Associated with Albright Hereditary Osteodystrophy
por: Sengupta, Sabyasachi, et al.
Publicado: (2012)

Heterotopic Ossifications in a Mouse Model of Albright Hereditary Osteodystrophy
por: Huso, David L., et al.
Publicado: (2011)

Case report: An infantile lethal form of Albright hereditary osteodystrophy due to a GNAS mutation
por: Leclercq, Valérie, et al.
Publicado: (2018)

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

Albright hereditary osteodystrophy: Delay in the diagnosis of a rare disorder due to restricted medical services
por: Noor, Sahar, et al.
Publicado: (2023)

2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance
por: Elli, Francesca Marta, et al.
Publicado: (2019)

Ostéodystrophie héréditaire d'Albright: à propos d'une observation
por: Tami, Laila, et al.
Publicado: (2019)

Methylation Defect in Imprinted Genes Detected in Patients with an Albright's Hereditary Osteodystrophy Like Phenotype and Platelet Gs Hypofunction
por: Izzi, Benedetta, et al.
Publicado: (2012)

PSAT183 Severe Hypocalcemia Precipitated by COVID-19 Infection in a Patient with Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism
por: Siddiqui, Samrah, et al.
Publicado: (2022)

Duplication of 17q11.2 and Features of Albright Hereditary Osteodystrophy Secondary to Methylation Defects within the GNAS Cluster: Coincidence or Causal?
por: White, M., et al.
Publicado: (2013)

Parental Origin of Gsα Inactivation Differentially Affects Bone Remodeling in a Mouse Model of Albright Hereditary Osteodystrophy
por: McMullan, Patrick, et al.
Publicado: (2021)

A patient with features of albright hereditory osteodystrophy and unusual neuropsychiatric findings without coding Gsalpha mutations
por: Hasani-Ranjbar, Shirin, et al.
Publicado: (2014)

Hypocalcemic Recurrent Generalized Seizures with Bilateral Basal Ganglia and Frontal Calcification as the Initial Manifestation of Albright’s Hereditary Osteodystrophy in a Child: A Pictorial and Video-graphic Representations
por: Nunavath, Akhilesh Kumar, et al.
Publicado: (2019)

Rickety Osteodystrophy
Publicado: (1935)

Osteodystrophies of jaws
por: Santana, N, et al.
Publicado: (2020)

Renal osteodystrophy in the obesity era: Is metabolic syndrome relevant?
por: Da Silva Martins, Janaina, et al.
Publicado: (2017)

A case report of McCune–Albright syndrome with hepatic manifestations
por: Haddadi, Mohammad, et al.
Publicado: (2022)

Otalgia revealing McCune-Albright syndrome: A case report
por: Sbai, Achraf Amine, et al.
Publicado: (2022)

McCune–Albright Syndrome: A Case Report and Review of Literature
por: Nicolaides, Nicolas C., et al.
Publicado: (2023)

Diagnosis and treatment of McCune-Albright syndrome: A case report
por: Lin, Xin, et al.
Publicado: (2023)

Case Report of a Satin Guinea Pig with Fibrous Osteodystrophy That Resembles Human Pseudohypoparathyroidism
por: Gallego, Miguel
Publicado: (2017)

Osteodystrophy from Cattle Disease
Publicado: (1931)

Parathyreoid Osteodystrophy (Osteitis Fibrosa)
por: Struthers, J. W.
Publicado: (1933)

Post-Traumatic Osteodystrophy at Joints
por: Middleton, D. Stewart, et al.
Publicado: (1934)

A Case of Primary Hypogonadism with Features of Albright’s Syndrome
por: Lodh, Moushumi, et al.
Publicado: (2016)

Neonatal McCune–Albright syndrome with systemic involvement: a case report
por: Lourenço, Rita, et al.
Publicado: (2015)

Epidural Hematoma after Minor Trauma on Patient with Biparietal Osteodystrophy
por: Yılmaz, Muhammet Bahadır, et al.
Publicado: (2013)

Hepatic osteodystrophy with hypophosphataemia and elevated fibroblast growth factor‐23
por: Ng, Nicholas Beng Hui, et al.
Publicado: (2022)

Albright's dimpling sign
por: Venkatesh, Chandrasekaran, et al.
Publicado: (2013)

Oral manifestations of McCune-Albright syndrome
por: Aravinda, Konidena, et al.
Publicado: (2013)

Hansen's disease with McCune–Albright syndrome
por: Kumar, KVS Hari, et al.
Publicado: (2012)

Delayed Diagnosis of McCune–Albright Syndrome
por: Fantahun, Bereket, et al.
Publicado: (2021)

Bone Canopies in Pediatric Renal Osteodystrophy
por: Pereira, Renata C., et al.
Publicado: (2016)

Cyst-like Tumors in Renal Osteodystrophy
por: Li Cavoli, Gioacchino, et al.
Publicado: (2021)

Bilateral spontaneous fracturing of the femoral neck in a patient with renal osteodystrophy()()
por: Garcia, Flavio Luís, et al.
Publicado: (2014)

Correction of Severe Knees Valgus Deformities in a Patient With Renal Osteodystrophy
por: Bytyqi, Cen, et al.
Publicado: (2022)

Radioiodine treatment in McCune–Albright syndrome with hyperthyroidism
por: Chakraborty, Dhritiman, et al.
Publicado: (2012)

McCune-Albright syndrome
por: Dumitrescu, Claudia E, et al.
Publicado: (2008)

McCune Albright Syndrome
por: Jibbe, Nada, et al.
Publicado: (2020)

Neonatal cholestasis can be the first symptom of McCune–Albright syndrome: A case report
por: Satomura, Yoshinori, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_v1u42cnfa98d9vqqqdc13q2uvk