Page last updated: 2024-10-17

salicylic acid and Noonan Syndrome

salicylic acid has been researched along with Noonan Syndrome in 3 studies

Scalp: The outer covering of the calvaria. It is composed of several layers: SKIN; subcutaneous connective tissue; the occipitofrontal muscle which includes the tendinous galea aponeurotica; loose connective tissue; and the pericranium (the PERIOSTEUM of the SKULL).

Noonan Syndrome: 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 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.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's1 (33.33)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Mercadante, F1
Piro, E1
Busè, M1
Salzano, E1
Ferrara, A1
Serra, G1
Passarello, C1
Corsello, G1
Piccione, M1
Van Kouwenberg, E1
Chattha, AS1
Adetayo, OA1
Kennedy, A1
Perry, D1
Battin, M1

Other Studies

3 other studies available for salicylic acid and Noonan Syndrome

ArticleYear
Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 gene.
    Italian journal of pediatrics, 2022, Aug-19, Volume: 48, Issue:1

    Topics: Humans; Noonan Syndrome; Rare Diseases; Scalp

2022
Improving Functional and Aesthetic Outcomes in Syndromic Patients With Webbed Neck Deformity: Utilizing a Staged Endoscopic-Assisted Approach to Improve the Posterior Hairline and Decrease Scar Burden.
    The Journal of craniofacial surgery, 2017, Volume: 28, Issue:4

    Topics: Adolescent; Child, Preschool; Endoscopy; Fasciotomy; Female; Humans; Neck; Noonan Syndrome; Range of

2017
Antenatal imaging of cutis verticis gyrata.
    Pediatric radiology, 2008, Volume: 38, Issue:5

    Topics: Cardiomyopathy, Hypertrophic; Diagnosis, Differential; Disease Progression; Fatal Outcome; Humans; I

2008