Cargando…

Prolonged thrombocytopenia in a neonate with Noonan syndrome: a case report

We report a case of a Chinese neonate who was diagnosed with Noonan syndrome and had persistent, self-limited thrombocytopenia. The neonate was admitted to the Neonatology Department 20 minutes after birth because of respiratory distress. From birth until 2 months of age, platelet values fluctuated...

Descripción completa

Detalles Bibliográficos
Autores principales:	Li, Meng, Zhang, Jinghui, Sun, Nianzheng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2020
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469734/ https://www.ncbi.nlm.nih.gov/pubmed/32867556 http://dx.doi.org/10.1177/0300060520936445

Ejemplares similares

Refractory thrombocytopenia could be a rare initial presentation of Noonan syndrome in newborn infants: a case report and literature review
por: Tang, Xiujun, et al.
Publicado: (2022)

Noonan syndrome with somnambulism: A rare case report
por: Sahu, Samiksha, et al.
Publicado: (2020)

The first reported case of Noonan syndrome complicated with hepatocellular carcinoma
por: Kakizaki, Satoru, et al.
Publicado: (2021)

Prenatal diagnosis of Noonan syndrome in a set of monozygotic twins- a case report
por: Jian, Wei, et al.
Publicado: (2023)

Management of Cardiovascular Disorders in Patients with Noonan Syndrome: A Case Report
por: Khorgami, Mohammad Rafie, et al.
Publicado: (2017)

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

A case of Noonan's syndrome with anomalous lymphorenal communication
por: Goli, Sanjeeva, et al.
Publicado: (2011)

Tisagenlecleucel: Prolonged neutropenia and thrombocytopenia: case report
Publicado: (2022)

Mutation in NRAS in familial Noonan syndrome – case report and review of the literature
por: Ekvall, Sara, et al.
Publicado: (2015)

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

A First Case Report of Subependymoma in PTPN11 Mutation-Associated Noonan Syndrome
por: Boonyawat, Boonchai, et al.
Publicado: (2019)

Anesthetic considerations and difficult airway management in a case of Noonan syndrome
por: Bajwa, Sukhminder Jit Singh, et al.
Publicado: (2011)

Multifocal Pigmented Villonodular Synovitis in the Noonan Syndrome
por: Miri, Othmane, et al.
Publicado: (2018)

Pulmonary Vasculitis and a Horseshoe Kidney in Noonan Syndrome
por: Puvabanditsin, Surasak, et al.
Publicado: (2018)

Thrombocytopenia with absent radii (TAR) syndrome in a female neonate: a case report
por: Alagbe, Olayemi Atinuke, et al.
Publicado: (2019)

Co‐occurrence of hypertrophic cardiomyopathy and juvenile myelomonocytic leukemia in a neonate with Noonan syndrome, leading to premature death
por: Tamura, Akihiro, et al.
Publicado: (2018)

Successful treatment of refractory chylothorax with MEK inhibitor trametinib in a child with Noonan syndrome: case report
por: Hribernik, Ines, et al.
Publicado: (2023)

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

A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature review
por: Zhao, Xiu, et al.
Publicado: (2021)

MAPK activation in mature cataract associated with Noonan syndrome
por: Hashida, Noriyasu, et al.
Publicado: (2013)

Multiple Unerupted Permanent Teeth Associated with Noonan Syndrome
por: Uloopi, KS, et al.
Publicado: (2015)

Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome
por: Vurallı, Doğuş, et al.
Publicado: (2016)

Periodontitis and Intra-Oral Plasmacytosis in a Noonan's Syndrome Patient
por: Alqatami, Hadeel, et al.
Publicado: (2022)

Out-of-hospital cardiac arrest and survival in a patient with Noonan syndrome and multiple lentigines: a case report
por: Eichhorn, Christian, et al.
Publicado: (2019)

Anterior Uveitis and Coats Disease in a 16-Year-Old Girl with Noonan Syndrome—A Case Report
por: Świerczyńska, Marta, et al.
Publicado: (2023)

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

Low-Grade Gliomas in Patients with Noonan Syndrome: Case-Based Review of the Literature
por: Lodi, Mariachiara, et al.
Publicado: (2020)

A case of Noonan syndrome with skull defect due to vitamin D deficiency rickets
por: Nagara, Syunsuke, et al.
Publicado: (2021)

An atypical case of Noonan syndrome with KRAS mutation diagnosed by targeted exome sequencing
por: Kim, Jinsup, et al.
Publicado: (2017)

Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 gene
por: Mercadante, Francesca, et al.
Publicado: (2022)

A rare mutation in a patient with Noonan syndrome with multiple lentigines
por: Blanco-Cintrón, Manuel E., et al.
Publicado: (2023)

Cubital tunnel syndrome in Noonan syndrome secondary to hypoplasia of the humeral trochlea
por: Koike, Mana, et al.
Publicado: (2020)

Disruption of the glomerular basement membrane associated with nutcracker syndrome and double inferior vena cava in Noonan syndrome: a case report
por: Omori, Ayumi, et al.
Publicado: (2022)

Case report: Noonan syndrome with protein-losing enteropathy
por: Ou, Yang, et al.
Publicado: (2023)

A neonate with marked prolonged mixed apneas and CHARGE syndrome: a case report
por: Riedijk, M. A., et al.
Publicado: (2018)

A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia
por: Işık, Esra, et al.
Publicado: (2020)

Anaesthesia for emergency ventriculo-peritoneal shunt in an adolescent with Noonan's syndrome
por: Samra, Tanvir, et al.
Publicado: (2014)

Late-onset Lymphedema and Protein-losing Enteropathy with Noonan Syndrome
por: Hasegawa, Kosei, et al.
Publicado: (2009)

Nonspecific phenotype of Noonan syndrome diagnosed by whole exome sequencing
por: Coromilas, Alexandra, et al.
Publicado: (2015)

Hashimoto thyroiditis with an unusual presentation of cardiac tamponade in Noonan syndrome
por: Lee, Mi Ji, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_lckdrji1hq05e7nb2q8eb75tjj