Clinical expertise includes: Hereditary Hemorrhagic Telangiectasia (HHT).
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Abnormal Genetic Test Results
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Arteriovenous Malformations (AVM)
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Autism
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BAP1 Gene
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Birth Defects and Disorders
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Cancer Predisposition Syndromes
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CDKN2A Gene
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Developmental Delay
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DICER1 Gene
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Familial Medullary Thyroid Cancer
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Family History of Autism
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Family History of Cancer
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Family History of Chromosomal Anomaly
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Family History of Intellectual Disabilities
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FLCN Gene
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Fragile X Syndrome
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Genetic Causes of Vascular Malformations
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Genetic Counseling
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Genetic Disorders
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Genetic Testing
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Gorlin Syndrome
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Hereditary Hemorrhagic Telangiectasia (HHT)
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Incontinentia Pigmenti
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Inherited Genetic Disorders
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Intellectual Disability
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KIT Gene
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Learning Disabilities
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Macrocephaly
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Marfan Syndrome
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MAX Gene
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MET Gene
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MET Proto-Oncogene Receptor Tyrosine Kinase Mutation
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MITF Gene
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Neurofibromatosis
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Polycystic Kidney Disease (PKD)
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Preventive Medicine
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PTCH1 Gene
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SDHAa Gene
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SDHAF2 Gene
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SDHB Gene
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SDHCGene
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SDHD Gene
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Second Opinion Service
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SMAD4 Gene
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SUFU Gene
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TMEM127 Gene
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Tuberous Sclerosis
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VHL Gene
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Programs and Centers
Penn Medicine's programs and centers combine doctors from many disciplines to coordinate care from start to finish. Ms. Raper is part of these programs: