Cargando…

Virginal breast hypertrophy in a patient with Beckwith–Wiedemann syndrome

Virginal breast hypertrophy is a multidisciplinary condition including surgical, pediatric, and endocrine/gynecological disciplines, and its successful diagnosis and management requires complex, team approach.

Detalles Bibliográficos
Autores principales:	Szymańska, Edyta, Moszczyńska, Elżbieta, Polnik, Dariusz, Szymańska, Sylwia, Jurkiewicz, Elżbieta, Pyzlak, Michał, Armata, Michał, Walewska‐Wolf, Małgorzata, Kaliciński, Piotr, Rokicki, Dariusz, Szalecki, Mieczysław
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2018
Materias:	Case Reports
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838282/ https://www.ncbi.nlm.nih.gov/pubmed/29531723 http://dx.doi.org/10.1002/ccr3.1362

Ejemplares similares

Beckwith-Wiedemann syndrome
por: Mishra, Deeksha, et al.
Publicado: (2023)

Ki67 as a prognostic factor of craniopharyngioma’s recurrence in paediatric population
por: Moszczyńska, Elżbieta, et al.
Publicado: (2020)

Sonographic Assessment of Renal Growth in Patients with Beckwith-Wiedemann Syndrome: The Beckwith-Wiedemann Syndrome Renal Nomogram
por: Ortiz-Neira, Clara L, et al.
Publicado: (2009)

Evidence for anticipation in Beckwith–Wiedemann syndrome
por: Berland, Siren, et al.
Publicado: (2013)

Diagnosis and Management of Beckwith-Wiedemann Syndrome
por: Wang, Kathleen H., et al.
Publicado: (2020)

Traditional and New Methods of Bone Age Assessment-An Overview
por: Prokop-Piotrkowska, Monika, et al.
Publicado: (2021)

Mild phenotype of glutaric aciduria type 1 in polish patients – novel data from a group of 13 cases
por: Pokora, Paulina, et al.
Publicado: (2018)

Tyrosinemia type III in an asymptomatic girl
por: Szymanska, Edyta, et al.
Publicado: (2015)

Validating mouse model of Beckwith-Wiedemann syndrome
Publicado: (2011)

Placental Mesenchymal Dysplasia and Beckwith–Wiedemann Syndrome
por: Soejima, Hidenobu, et al.
Publicado: (2022)

Pathogenesis of chronic constipation in a Polish group of paediatric patients – an attempt to create the optimal histopathological diagnostic protocol
por: Szymańska, Sylwia, et al.
Publicado: (2019)

Tissue Expression of Programmed Cell Death 1 Ligand1 (PD-L1) in Biopsies of Transplant Livers of Pediatric Patients as a Possible Marker of Acute Cellular Rejection
por: Szymanska, Sylwia, et al.
Publicado: (2023)

Meningocele in a Congolese Female with Beckwith-Wiedemann Phenotype
por: Mbuyi-Musanzayi, Sébastien, et al.
Publicado: (2014)

Beckwith–Wiedemann syndrome and recurrent bilateral renal calculi
por: Cheungpasitporn, Wisit, et al.
Publicado: (2017)

A rare case of Beckwith-Wiedemann syndrome with encephalocele
por: Khatana, Rakesh, et al.
Publicado: (2020)

Occurrence of Hepatoblastomas in Patients with Beckwith–Wiedemann Spectrum (BWSp)
por: Klein, Steven D., et al.
Publicado: (2023)

Introduction to the Beckwith–Wiedemann Syndrome and Cancer Special Issue
por: Mussa, Alessandro, et al.
Publicado: (2023)

Multiple Fractures in an Infant With Hepatoblastoma and Beckwith-Wiedemann Syndrome
por: Eimicke, Toni, et al.
Publicado: (2023)

Variable clinical presentation of glycogen storage disease type IV: from severe hepatosplenomegaly to cardiac insufficiency. Some discrepancies in genetic and biochemical abnormalities
por: Szymańska, Edyta, et al.
Publicado: (2017)

Over 20-Year Follow-up of Patients with Hepatic Glycogen Storage Diseases: Single-Center Experience
por: Szymańska, Edyta, et al.
Publicado: (2020)

Pediatric patient with hyperketotic hypoglycemia diagnosed with glycogen synthase deficiency due to the novel homozygous mutation in GYS2
por: Szymańska, Edyta, et al.
Publicado: (2015)

Genetic diagnosis of Beckwith Wiedemann syndrome and Silver-Russell syndrome
por: Kim, Yoo-Mi, et al.
Publicado: (2013)

Cystic Fibrosis and Beckwith-Wiedemann Syndrome: A Case Report
por: Aguiar, Claudia, et al.
Publicado: (2015)

Perioperative airway management of a patient with Beckwith-Wiedemann syndrome
por: Tsukamoto, Masanori, et al.
Publicado: (2016)

Preclinical and Clinical Epigenetic-Based Reconsideration of Beckwith-Wiedemann Syndrome
por: Papulino, Chiara, et al.
Publicado: (2020)

Macroglossia in Beckwith-Wiedemann Syndrome Is Attributed to Skeletal Muscle Hyperplasia
por: Oyama, Yuzo, et al.
Publicado: (2020)

Phenotypes and epigenetic errors in patients with Beckwith-Wiedemann syndrome in China
por: Zhang, Miaoying, et al.
Publicado: (2020)

Adrenocortical adenoma in a Sudanese girl with Beckwith-Wiedemann syndrome
por: Elnaw, Eman Abdalla Ali, et al.
Publicado: (2019)

MON-LB036 Uncommon Findings in Beckwith-Wiedemann Syndrome
por: Martins, Jéssica M E S, et al.
Publicado: (2020)

Functional Adrenocortical Adenoma in a Child with Beckwith–Wiedemann Syndrome
por: Doya, Leen Jamel, et al.
Publicado: (2021)

Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith‐Wiedemann syndrome
por: Sobel Naveh, Natali S., et al.
Publicado: (2022)

Metastatic Phyllodes Tumor in a Patient With Beckwith-Wiedemann Syndrome
por: Saini, Astha, et al.
Publicado: (2022)

Recurrent Hypoglycemia Secondary to Insulinoma in an Adult With Beckwith-Wiedemann Syndrome
por: Akcan, Tugce, et al.
Publicado: (2023)

Treatment challenges in pediatric Cushing’s disease: Review of the literature with particular emphasis on predictive factors for the disease recurrence
por: Pasternak-Pietrzak, Katarzyna, et al.
Publicado: (2019)

The quality of life in adult patients treated for Cushing’s disease in childhood
por: Pasternak-Pietrzak, Katarzyna, et al.
Publicado: (2021)

Ectopic virilising adrenocortical tumour in the spinal region in an 8 year-old boy: a case report and review of the literature
por: Skórka, Agata, et al.
Publicado: (2015)

Liver Histopathology in Late Protocol Biopsies after Pediatric Liver Transplantation
por: Markiewicz-Kijewska, Małgorzata, et al.
Publicado: (2021)

Long Term Follow-Up of Polish Patients with Isovaleric Aciduria. Clinical and Molecular Delineation of Isovaleric Aciduria
por: Szymańska, Edyta, et al.
Publicado: (2020)

Outcomes of oral biotin treatment in patients with biotinidase deficiency — Twenty years follow-up
por: Szymańska, Edyta, et al.
Publicado: (2015)

Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome
por: Oh-McGinnis, Rosemary, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_l1ghvg2ibqd2vtb602d97pgfko