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Up to: Syndromic disease · Autosomal dominant disease · Multiple congenital anomalies/dysmorphic syndrome without intellectual disability · Noonan syndrome and Noonan-related syndrome
Noonan syndrome with multiple lentigines
A rare multisystem genetic disorder characterized by lentigines, hypertrophic cardiomyopathy, short stature, pectus deformity, and dysmorphic facial features.
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LEOPARD syndrome 1 0 trials
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LEOPARD syndrome 2 0 trials
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LEOPARD syndrome 3 0 trials