"Noonan Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A genetically heterogeneous, multifaceted disorder characterized by short stature, webbed neck, ptosis, skeletal malformations, hypertelorism, hormonal imbalance, CRYPTORCHIDISM, multiple cardiac abnormalities (most commonly including PULMONARY VALVE STENOSIS), and some degree of INTELLECTUAL DISABILITY. The phenotype bears similarities to that of TURNER SYNDROME that occurs only in females and has its basis in a 45, X karyotype abnormality. Noonan syndrome occurs in both males and females with a normal karyotype (46,XX and 46,XY). Mutations in a several genes (PTPN11, KRAS, SOS1, NF1 and RAF1) have been associated the the NS phenotype. Mutations in PTPN11 are the most common. LEOPARD SYNDROME, a disorder that has clinical features overlapping those of Noonan Syndrome, is also due to mutations in PTPN11. In addition, there is overlap with the syndrome called neurofibromatosis-Noonan syndrome due to mutations in NF1.
Descriptor ID |
D009634
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MeSH Number(s) |
C05.660.207.690 C14.240.400.787 C14.280.400.787 C16.131.240.400.784 C16.131.621.207.690 C17.300.690
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Concept/Terms |
Noonan Syndrome- Noonan Syndrome
- Syndrome, Noonan
- Noonan Syndrome 1
- Noonan-Ehmke Syndrome
- Noonan Ehmke Syndrome
- Syndrome, Noonan-Ehmke
- Pseudo-Ullrich-Turner Syndrome
- Pseudo Ullrich Turner Syndrome
- Syndrome, Pseudo-Ullrich-Turner
- Turner's Phenotype, Karyotype Normal
- Turner-Like Syndrome
- Syndrome, Turner-Like
- Turner Like Syndrome
- Ullrich-Noonan Syndrome
- Syndrome, Ullrich-Noonan
- Ullrich Noonan Syndrome
- Familial Turner Syndrome
- Syndrome, Familial Turner
- Turner Syndrome, Familial
- Turner Phenotype with Normal Karyotype
Female Pseudo-Turner Syndrome- Female Pseudo-Turner Syndrome
- Female Pseudo Turner Syndrome
- Pseudo-Turner Syndrome, Female
- Syndrome, Female Pseudo-Turner
Turner Syndrome, Male- Turner Syndrome, Male
- Syndrome, Male Turner
- Turner's Syndrome, Male
- Male Turner's Syndrome
- Syndrome, Male Turner's
- Male Turner Syndrome
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Below are MeSH descriptors whose meaning is more general than "Noonan Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Noonan Syndrome".
This graph shows the total number of publications written about "Noonan Syndrome" by people in this website by year, and whether "Noonan Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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2000 | 1 | 0 | 1 |
2002 | 1 | 0 | 1 |
2008 | 1 | 0 | 1 |
2009 | 2 | 0 | 2 |
2010 | 2 | 0 | 2 |
2012 | 1 | 0 | 1 |
2014 | 2 | 0 | 2 |
2016 | 2 | 0 | 2 |
2018 | 1 | 0 | 1 |
2019 | 2 | 0 | 2 |
2022 | 2 | 0 | 2 |
2023 | 1 | 0 | 1 |
2024 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Noonan Syndrome" by people in Profiles.
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Update on Pediatric Cancer Surveillance Recommendations for Patients with Neurofibromatosis Type 1, Noonan Syndrome, CBL Syndrome, Costello Syndrome, and Related RASopathies. Clin Cancer Res. 2024 Nov 01; 30(21):4834-4843.
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The 8th International RASopathies Symposium: Expanding research and care practice through global collaboration and advocacy. Am J Med Genet A. 2024 04; 194(4):e63477.
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Transient abnormal lymphomyelopoiesis in a newborn with PTPN11 mutation associated Noonan syndrome. Cytometry B Clin Cytom. 2022 09; 102(5):409-411.
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The seventh international RASopathies symposium: Pathways to a cure-expanding knowledge, enhancing research, and therapeutic discovery. Am J Med Genet A. 2022 06; 188(6):1915-1927.
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RASopathies: A significant cause of polyhydramnios? Prenat Diagn. 2021 02; 41(3):362-367.
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Cardiac transplantation in children with Noonan syndrome. Pediatr Transplant. 2019 09; 23(6):e13535.
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Impact of Noonan Syndrome on admissions for pediatric cardiac surgery. Minerva Pediatr (Torino). 2022 08; 74(4):461-467.
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Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants. Genet Med. 2018 10; 20(10):1175-1185.
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Further evidence that variants in PPP1CB cause a rasopathy similar to Noonan syndrome with loose anagen hair. Am J Med Genet A. 2017 02; 173(2):565-567.
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Childhood Rhabdomyosarcoma in Association With a RASopathy Clinical Phenotype and Mosaic Germline SOS1 Duplication. J Pediatr Hematol Oncol. 2016 11; 38(8):e278-e282.