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Readers' pathsAug 2026 – Oct 2026
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Noonan syndrome
Genetic condition involving facial, heart, blood and skeletal features.
22%
Westerhof syndrome
Medical condition.
21%
Lisch nodule
Small growths on the iris of the eye.
14%
Pulmonary valve stenosis
Heart valve disorder.
12%
Neurofibromatosis type I
Type of neurofibromatosis disease.
7.9%
Neurofibroma
Benign nerve-sheath tumor in the peripheral nervous system.
2.9%
Genetic disorder
Health problem from genome abnormalities.
2.6%
Readers come from
Share of the 1,811 readers arriving from another article
Noonan syndrome
Genetic condition involving facial, heart, blood and skeletal features.
65%
Neurofibromatosis type I
Type of neurofibromatosis disease.
19%
Café au lait spot
Type of birthmark caused by a collection of melanocytes.
5%
Lisch nodule
Small growths on the iris of the eye.
3%
Neurofibromin
Mammalian protein found in humans.
1.4%
Neurofibroma
Benign nerve-sheath tumor in the peripheral nervous system.
0.61%