Cargando…

Multiple endocrine glands insufficiency due to langerhans cell histiocytosis (LCH): a case report

Detalles Bibliográficos
Autores principales:	Mai, DoThi Thanh, Dung, Vu Chi, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Dat, Nguyen Phu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2015
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428786/ http://dx.doi.org/10.1186/1687-9856-2015-S1-P119

Ejemplares similares

Congenital adrenal hyperplasia with cholestatic jaundice: a case report
por: Mai, DoThi Thanh, et al.
Publicado: (2015)

Hypopituitarism due to central nervous system germinoma: a case report
por: Mai, DoThi Thanh, et al.
Publicado: (2015)

Primary hyperlipidemia in children: clinical, biochemistry characteristics and outcome
por: Khanh, Nguyen Ngoc, et al.
Publicado: (2015)

Adrenal cortex tumors: clinical features and laboratory finding
por: Ngoc, Can Thi Bich, et al.
Publicado: (2013)

Mutations of ABCD1 gene and phenotype of Vietnamese patients with X-linked adrenoleukodystrophy (X-ALD)
por: Dung, Vu Chi, et al.
Publicado: (2013)

Phenotype & genotype of congenital adrenal hyperplasia due to mutation in the type ii 3β-hydroxysteroid dehydrogenase gene: a report of two Vietnamese families
por: Dung, Vu Chi, et al.
Publicado: (2015)

Updated registry of congenital adrenal hyperplasia at the north pediatric referral centre of Vietnam
por: Dung, Vu Chi, et al.
Publicado: (2015)

Treatment outcome and some affecting factors of congenital adrenalhyperplasia
por: Dat, Nguyen Phu, et al.
Publicado: (2013)

Study relationship between the value of 17-OHP and the value of testosterone in monitoring for congenital adrenal hyperplasia
por: Huong, Ngo Thi Thu, et al.
Publicado: (2013)

Factors affecting on the mental development in children with Congenital Hypothyroidism
por: Dat, Nguyen Phu, et al.
Publicado: (2013)

The pattern of disorders of sex development in Vietnamese children
por: Nga, Pham Thu, et al.
Publicado: (2015)

Phenotype of patients with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
por: Dung, Vu Chi, et al.
Publicado: (2015)

Novel mutation in the hepatocyte nuclear factor 1B/maturity – onset diabetes of the young type 5 gene – unreported Vietnamese case
por: Dung, Vu Chi, et al.
Publicado: (2015)

Phenotype, genotype of neonatal diabetes mellitus due to insulin gene mutation
por: Ngoc, Can Thi Bich, et al.
Publicado: (2015)

Eye and renal complication in pediatric patients with diabetes mellitus type 1
por: Hieu, Nguyen Tran Ngoc, et al.
Publicado: (2015)

Hepatic Langerhans Cell Histiocytosis (LCH) Presenting as a Harbinger of Multisystem LCH
por: Li, Hua, et al.
Publicado: (2020)

Effect of osteogenesis imperfecta on children and their families
por: Dung, Vu Chi, et al.
Publicado: (2013)

Molecular genetics and phenotype of 26 Vietnamese patients with congenital hyperinsulinism
por: Dung, Vu Chi, et al.
Publicado: (2013)

Clinical and laboratory characteristics of Prader-Willi syndrome
por: Thao, Bui Phuong, et al.
Publicado: (2013)

Genotype and phenotype of Vietnamese patients with androgen insensitivity syndrome
por: Dung, Vu Chi, et al.
Publicado: (2013)

Molecular genetics, correlation between genotype and phenotype of 65 Vietnames patients with congenital hyperinsulinism
por: Duong, Dang Anh, et al.
Publicado: (2015)

Phenotype and genotype of patients with disorder of sex development due to 5α-reductase deficiency
por: Dung, Vu Chi, et al.
Publicado: (2015)

Mixed embryonal carcinoma – teratoma cause early puberty: a case report
por: Ngoc, Can Thi Bich, et al.
Publicado: (2015)

Pseudoaldosteronism due to mutation of SCNN1A gene: a case report
por: Ngoc, Can Thi Bich, et al.
Publicado: (2015)

Hearing loss in osteogenesis imperfecta patients
por: Ha, Lai Thu, et al.
Publicado: (2015)

Plasma Signaling Factors in Patients With Langerhans Cell Histiocytosis (LCH) Correlate With Relative Frequencies of LCH Cells and T Cells Within Lesions
por: Mitchell, Jenée, et al.
Publicado: (2022)

A case report of neonatal adrenocortical carcinoma
por: Thao, Bui Phuong, et al.
Publicado: (2015)

Adrenocortical tumor in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
por: Dung, Vu Chi, et al.
Publicado: (2015)

Polyclonal T-Cells Express CD1a in Langerhans Cell Histiocytosis (LCH) Lesions
por: West, Jennifer A., et al.
Publicado: (2014)

Langerhans-cell histiocytosis (LCH) a presentation of two siblings with two different entities
por: Aboud, Mohammed Joudi, et al.
Publicado: (2015)

Spinal epidural involvement in adult Langerhans cell histiocytosis (LCH): A case report
por: Lim, Cheong-Su, et al.
Publicado: (2020)

Clinical, para-clincal and outcomes of diabetes ketoacidosis in Vietnam national hospital pediatrics
por: Nga, Nguyen Thi Thu, et al.
Publicado: (2015)

Molecular Analysis of Vietnamese Patients with Mucopolysaccharidosis Type I
por: Can, Ngoc Thi Bich, et al.
Publicado: (2021)

Genetic Etiology of Neonatal Diabetes Mellitus in Vietnamese Infants and Characteristics of Those With INS Gene Mutations
por: Ngoc, Can Thi Bich, et al.
Publicado: (2022)

Pilot study to estimate the safety and effectiveness of hydroxyurea and methotrexate recurrent langerhans cell histiocytosis (LCH-HU-pilot)
por: Sakamoto, Kenichi, et al.
Publicado: (2022)

Evaluation of parental knowledge after establishing CAH clubs in Vietnam & Indonesia
por: Mitchelhill, Irene, et al.
Publicado: (2015)

Langerhans Cell Histiocytosis (LCH): Guidelines for Diagnosis, Clinical Work-Up, and Treatment for Patients Till the Age of 18 Years
por: Haupt, Riccardo, et al.
Publicado: (2013)

PB2491: LANGERHANS CELL HISTIOCYTOSIS (LCH) IN THE MAXILLOFACIAL AREA IN ADULT. COMPLETE REMISSION WITH CLADRIBINE. CASE REPORT AND REVIEW.
por: De Miguel Llorente, Dunia, et al.
Publicado: (2023)

Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of K(ATP)-Channel Neonatal Diabetes Mellitus in Vietnam National Children’s Hospital
por: Ngoc, Can Thi Bich, et al.
Publicado: (2021)

Whole Exome Sequencing as a Diagnostic Tool for Unidentified Muscular Dystrophy in a Vietnamese Family
por: Nguyen, Ngoc-Lan, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_r1ofo89h42a36sseas4cvhrunl