Adeline Vanderver, MD
Rare Disease Specialist
Children's Hospital of Philadelphia
Los Angeles, California
PI on 4 trials 1 publication
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Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.
Report missing dataRare diseases treated or studied
Based on trial PI assignments and publication topics.
- Optic atrophy-intellectual disability syndrome
- Cockayne syndrome
- Genetic malformation syndrome with short stature
- Canavan disease
- Leukodystrophy
- GM2 gangliosidosis
- Aicardi-Goutières syndrome
- Multiple sulfatase deficiency
- Inherited ichthyosis
- Hypomyelination with brain stem and spinal cord involvement and leg spasticity
- Immune deficiency with skin involvement
- Genetic immune deficiency with skin involvement
- Charcot-Marie-Tooth disease type 1
- Pelizaeus-Merzbacher-like disease
- Adult Refsum disease
- Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy
- X-linked Charcot-Marie-Tooth disease
- Metabolic disease with skin involvement
- X-linked Charcot-Marie-Tooth disease type 5
- Null syndrome
- X-linked cerebral adrenoleukodystrophy
- Megalencephalic leukoencephalopathy with subcortical cysts
- Tay-Sachs disease
- Disorder of sialic acid metabolism
- Charcot-Marie-Tooth disease type 4H
- Hypomyelination with atrophy of basal ganglia and cerebellum
- Zellweger syndrome
- X-linked Charcot-Marie-Tooth disease type 1
- Gangliosidosis
- X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome
Clinical trials (4)
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