Patient Information

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Patient Handout Title
Palmoplantar Keratoderma and Woolly Hair
Pantothenate Kinase-Associated Neurodegeneration
Papillorenal Syndrome
Pearson Marrow-Pancreas Syndrome
PEHO Syndrome
PEHO-Like Syndrome
Pelizeaus-Merzbacher Disease
Peroxisome Biogenesis Disorder 1A (Zellweger)
Peroxisome Biogenesis Disorder 1B (neonatal adrenoleukodystrophy)
Peroxisome Biogenesis Disorder 3B (Infantile Refsum Disease)
Peroxisomol Fatty Acyl-CoA Reductase 1 Disorder
Perrault Syndrome
Persistent Hyperplastic Primary Vitreous
Peters Anomaly
Peters-Plus Syndrome
Pfeiffer Syndrome
Pierson Syndrome
Pigmentary Retinopathy with Congenital Sideroblastic Anemia
Pigmented Paravenous Chorioretinal Atrophy
Pontocerebellar Hypoplasia 11
Pontocerebellar Hypoplasia 3
Pontocerebellar Hypoplasia 7
Potter Disease, Type I
Progeroid Short Stature with Pigmented Nevi
Pseudohypoparathyroidism, Type 1A

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