Cargando…

Lymphatic anomalies during lifetime in patients with Noonan syndrome: Retrospective cohort study

Noonan syndrome (NS) has been associated with an increased risk of lymphatic anomalies, with an estimated prevalence of 20%. The prevalence of lymphatic anomalies seems to differ between pathogenic variants. Therefore, this study aims to describe the clinical presentation, prevalence and genotype–ph...

Descripción completa

Detalles Bibliográficos
Autores principales:	Swarts, Jessie W., Kleimeier, Lotte E. R., Leenders, Erika K. S. M, Rinne, Tuula, Klein, Willemijn M., Draaisma, Jos M. T.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley & Sons, Inc. 2022
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804719/ https://www.ncbi.nlm.nih.gov/pubmed/35979676 http://dx.doi.org/10.1002/ajmg.a.62955

Ejemplares similares

Lymphatic Phenotype of Noonan Syndrome: Innovative Diagnosis and Possible Implications for Therapy
por: Kleimeier, Lotte E. R., et al.
Publicado: (2022)

Hypertrophic neuropathy: a possible cause of pain in children with Noonan syndrome and related disorders
por: Draaisma, Fieke, et al.
Publicado: (2023)

Young children with Noonan syndrome: evaluation of feeding problems
por: Draaisma, Jos M. T., et al.
Publicado: (2020)

The most important problems and needs of rasopathy patients with a noonan syndrome spectrum disorder
por: Tiemens, Dagmar K., et al.
Publicado: (2023)

Feeding Problems in Patients with Noonan Syndrome: A Narrative Review
por: Tiemens, Dagmar K., et al.
Publicado: (2022)

Patient engagement in the design of clinical research in Noonan syndrome spectrum disorders: a scoping review
por: Tiemens, Dagmar K., et al.
Publicado: (2021)

Ocular findings in Noonan syndrome: a retrospective cohort study of 105 patients
por: van Trier, Dorothée C., et al.
Publicado: (2018)

Cognitive Phenotype and Psychopathology in Noonan Syndrome Spectrum Disorders through Various Ras/MAPK Pathway Associated Gene Variants
por: Wingbermühle, Ellen, et al.
Publicado: (2022)

High energy expenditure in a patient with feeding problems and Noonan syndrome spectrum disorder
por: Tiemens, Dagmar, et al.
Publicado: (2022)

Combined cardiac anomalies in Noonan syndrome: A case report
por: H.S., Natraj Setty, et al.
Publicado: (2020)

MR lymphangiography of lymphatic abnormalities in children and adults with Noonan syndrome
por: Pieper, C. C., et al.
Publicado: (2022)

Twin Infant with Lymphatic Dysplasia Diagnosed with Noonan Syndrome by Molecular Genetic Testing
por: Mathur, Deepan, et al.
Publicado: (2014)

The lymphatic system throughout history: From hieroglyphic translations to state of the art radiological techniques
por: van Schaik, Caroline J., et al.
Publicado: (2022)

Multimodality lymphatic imaging of postoperative chylothorax in an infant with Noonan syndrome: a case report
por: Pham, Kay T., et al.
Publicado: (2020)

Differences in severity of cardiovascular anomalies in children with Noonan syndrome based on the causative gene
por: Shehade-Awwad, Nagham, et al.
Publicado: (2022)

Tegumentary manifestations of Noonan and Noonan-related syndromes
por: Quaio, Caio Robledo D'Angioli Costa, et al.
Publicado: (2013)

Personality and Psychopathology in Adults with Noonan Syndrome
por: Roelofs, Renée L., et al.
Publicado: (2019)

Can digital X-ray radiogrammetry be an alternative for dual-energy X-ray absorptiometry in the diagnosis of secondary low bone quality in children?
por: Leijten, Alex D., et al.
Publicado: (2019)

Osteopathy in Complex Lymphatic Anomalies
por: Solorzano, Ernesto, et al.
Publicado: (2022)

Noonan syndrome
por: van der Burgt, Ineke
Publicado: (2007)

Intellectual development in Noonan syndrome: a longitudinal study
por: Roelofs, Renée L., et al.
Publicado: (2016)

Intestinal Manifestations of Generalized Lymphatic Anomaly
por: Okamoto, Takeshi, et al.
Publicado: (2020)

Transcriptional Hallmarks of Noonan Syndrome and Noonan-Like Syndrome with Loose Anagen Hair
por: Ferrero, Giovanni Battista, et al.
Publicado: (2012)

Social cognitive training for adults with Noonan syndrome: a feasibility study
por: Roelofs, Renée L, et al.
Publicado: (2019)

Severe Lymphatic Disorder and Multifocal Atrial Tachycardia Treated with Trametinib in a Patient with Noonan Syndrome and SOS1 Mutation
por: Lioncino, Michele, et al.
Publicado: (2022)

Genotypic Findings in Noonan and Non-Noonan RASopathies and Patient Eligibility for Growth Hormone Treatment
por: Carcavilla, Atilano, et al.
Publicado: (2023)

Unusual Intestinal Lesions of Generalized Lymphatic Anomaly
por: Koba, Taro, et al.
Publicado: (2020)

Neonatal Generalized Lymphatic Anomaly with Skin Involvement
por: Markovic-Sovtic, Gordana, et al.
Publicado: (2021)

Thoracic involvement in generalised lymphatic anomaly (or lymphangiomatosis)
por: Luisi, Francesca, et al.
Publicado: (2016)

Investigation into the genetics of fetal congenital lymphatic anomalies
por: Rogerson, Daniella, et al.
Publicado: (2023)

Clinical manifestations of Noonan syndrome
por: Digilio, MC, et al.
Publicado: (2001)

Recognition Memory in Noonan Syndrome
por: Costanzo, Floriana, et al.
Publicado: (2021)

Profound and selective lymphopaenia in primary lymphatic anomaly patients demonstrates the significance of lymphatic-lymphocyte interactions
por: Pearce, Julian, et al.
Publicado: (2023)

Effect of Growth Hormone Therapy in Patients with Noonan Syndrome: A Retrospective Study
por: Apperley, Louise Jayne, et al.
Publicado: (2020)

Lifetime of the $B^+_c$ meson in relation to flavour anomalies
por: Grinstein, Benjamin
Publicado: (2022)

The other side of Turner's: Noonan's syndrome
por: Agarwal, Pankaj, et al.
Publicado: (2013)

Noonan syndrome – a new survey
por: Tafazoli, Alireza, et al.
Publicado: (2016)

Noonan syndrome: improving recognition and diagnosis
por: Zenker, Martin, et al.
Publicado: (2022)

A case of haemoptysis in a girl with Noonan syndrome
por: Mopeli, R K, et al.
Publicado: (2020)

Erythematous capillary-lymphatic malformations mimicking blood vascular anomalies
por: Hägerling, René, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_qkrrv1g4hsd3q9on28nnva717t