Cargando…

Kostmann Syndrome With Neurological Abnormalities: A Case Report and Literature Review

Background: Severe congenital neutropenia (SCN), also known as Kostmann syndrome, is a rare heterogeneous group of diseases characterized by arrested neutrophil maturation in the bone marrow. Case Presentation: We report a case of Kostmann syndrome and review previously reported SCN cases with neuro...

Descripción completa

Detalles Bibliográficos
Autores principales:	Lyu, Baiyu, Lyu, Wei, Zhang, Xiaoying
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2020
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767819/ https://www.ncbi.nlm.nih.gov/pubmed/33381479 http://dx.doi.org/10.3389/fped.2020.586859

Ejemplares similares

Burnout syndrome, doctor-patient relationship and family support of pediatric medical staff during a COVID-19 Local outbreak in Shanghai China: A cross-sectional survey study
por: Lyu, Baiyu, et al.
Publicado: (2023)

Kostmann’s disease or severe hereditary neutropenia—the man behind the syndrome
por: Stenhammar, Lars, et al.
Publicado: (2020)

A New Case of de novo Variant c.892C>T (p.Arg298Trp) in NACC1: A First Case Report From China
por: Lyu, Baiyu, et al.
Publicado: (2021)

A Rare Case of Kostmann Syndrome Presenting Difficult Airway Challenges and Patient Preparedness for Anesthesiologists
por: Uppalapati, Vamsi Krishna, et al.
Publicado: (2022)

A Case of Papillary Thyroid Carcinoma and Kostmann Syndrome: A Genomic Theranostic Approach for Comprehensive Treatment
por: Han, Soo, et al.
Publicado: (2019)

Atypical Neurological Manifestation in Childhood Microscopic Polyangiitis: A Case Report and Review of Literature
por: Suksai, Preawkalaya, et al.
Publicado: (2022)

Case Report: A Case Report and Literature Review of 3p Deletion Syndrome
por: Fu, Junxian, et al.
Publicado: (2021)

Neurological Neonatal Birth Injuries: A Literature Review
por: Ojumah, Naomi, et al.
Publicado: (2017)

Myhre Syndrome Associated With Dunbar Syndrome and Urinary Tract Abnormalities: A Case Report
por: Varenyiova, Zofia, et al.
Publicado: (2020)

Neuroimaging of Propofol Infusion Syndrome: A Case Report and Review of Literature
por: Pernicone, Elizabeth, et al.
Publicado: (2020)

Juvenile dermatomyositis and nephrotic syndrome: A case report and a mini literature review
por: Zhou, Weiran, et al.
Publicado: (2023)

Autoimmune Encephalitis and Other Neurological Syndromes With Rare Neuronal Surface Antibodies in Children: A Systematic Literature Review
por: Ancona, Claudio, et al.
Publicado: (2022)

Case report: Two cases of Poirier-Bienvenu neurodevelopmental syndrome and review of literature
por: Chen, Xiaolan, et al.
Publicado: (2023)

Report of a Fatal Case of Hemophagocytic Lymphohistiocytosis Syndrome and a Review of the Literature
por: Khan, Hamza H, et al.
Publicado: (2020)

Growth Concerns in Coffin–Lowry Syndrome: A Case Report and Literature Review
por: Lv, Ying, et al.
Publicado: (2019)

Blau syndrome with hypertension and hepatic granulomas: a case report and literature review
por: Yao, Fangling, et al.
Publicado: (2023)

A Chinese family with cat eye syndrome and abnormality of eye movement: First case report
por: Lu, Yang, et al.
Publicado: (2023)

Lupus podocytopathy and antiphospholipid syndrome in a child with SLE: A case report and literature review
por: Li, Guo-min, et al.
Publicado: (2022)

Kawasaki Disease Complicated With Macrophage Activation Syndrome: Case Reports and Literature Review
por: Jin, Ping, et al.
Publicado: (2019)

Mexiletine Treatment for Neonatal LQT3 Syndrome: Case Report and Literature Review
por: Bagkaki, Alena, et al.
Publicado: (2021)

DICER1 syndrome and embryonal rhabdomyosarcoma of the cervix: a case report and literature review
por: Stambouli, Alexandre, et al.
Publicado: (2023)

Case Report: Fanconi-Bickel Syndrome in a Chinese Girl With Diabetes and Severe Hypokalemia
por: Chen, Hongbo, et al.
Publicado: (2022)

Literature review, report, and analysis of genotype and clinical phenotype of a rare case of ulnar-mammary syndrome
por: Zhang, Xiwen, et al.
Publicado: (2023)

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

Cantrell Syndrome—A Rare Complex Congenital Anomaly: A Case Report and Literature Review
por: Mărginean, Claudiu, et al.
Publicado: (2018)

Sudden cardiac arrest in a child with Gitelman syndrome: a case report and literature review
por: Zieg, Jakub, et al.
Publicado: (2023)

Case Report: Clinical Analysis of Seven Neonates With Prader-Willi Syndrome and Review of the Literature
por: Hu, Yu, et al.
Publicado: (2021)

A case of double cystic esophageal duplication in VACTERL syndrome: the first case report and a review of the literature
por: Vasta, G., et al.
Publicado: (2023)

Noonan syndrome caused by RIT1 gene mutation: A case report and literature review
por: Zha, Ping, et al.
Publicado: (2022)

Hutchinson-Gilford progeria syndrome complicated with stroke: A report of 2 cases and literature review
por: Wang, Jingjing, et al.
Publicado: (2022)

Galloway–Mowat Syndrome Type 3 Caused by OSGEP Gene Variants: A Case Report and Literature Review
por: Xu, Suhua, et al.
Publicado: (2022)

A Rare Case of an Asymmetric Overgrowth Syndrome in a Kenyan African Child: A Case Report and Review of Literature
por: Okello, Diana A, et al.
Publicado: (2022)

Case report: A rare case of pediatric female bladder neck obstruction
por: Lyu, Xuexue, et al.
Publicado: (2023)

Multicentric Carpo-Tarsal Osteolysis Syndrome Mimicking Juvenile Idiopathic Arthritis: Two Case Reports and Review of the Literature
por: Wu, Junfeng, et al.
Publicado: (2021)

Floating-Harbor Syndrome Treated With Recombinant Human Growth Hormone: A Case Report and Literature Review
por: Bo, Hui, et al.
Publicado: (2021)

Anti-AQP4–IgG-positive Leigh syndrome: A case report and review of the literature
por: Chen, Jun, et al.
Publicado: (2023)

Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review
por: Pavone, Piero, et al.
Publicado: (2023)

Case Report: Macrophage Activation Syndrome and Widespread Neuroimaging Abnormality in Childhood-Onset Systemic Lupus Erythematosus
por: Shi, Nana, et al.
Publicado: (2021)

Gorlin-Goltz Syndrome: A Case Report and Literature Review
por: Al-Jarboua, Maha N, et al.
Publicado: (2019)

Kidney teratoma: A case report and literature review
por: Chu, Han, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_mdrl3vg6kue1hlotcjlngeijgg