AccessAnesthesiology | Syndromes: Rapid Recognition and Perioperative Implications

Syndromes: Rapid Recognition and Perioperative Implications

Bruno Bissonnette, Igor Luginbuehl, Bruno Marciniak, Bernard J. Dalens

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A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

- Pachydermoperiostosis (PDP)
- PAGOD Syndrome
- Pallister-Hall Syndrome
- Papillon-Lefèvre Syndrome
- Parana Hard Skin Syndrome
- Paroxysmal Cold Hemoglobinuria
- Paroxysmal Nocturnal Hemolytic (PNH) Anemia
- Parry-Romberg Syndrome
- Patterson Pseudo-Leprechaunism Syndrome
- Pearson Syndrome
- Pectus Excavatum
- Pelizaeus-Merzbacher Syndrome
- Pemphigoid
- Pemphigus
- Pena-Shokeir Syndrome Type I
- Pena-Shokeir Syndrome Type II
- Pendred Syndrome
- Penta X Syndrome
- Pentalogy of Cantrell
- Pentosuria
- PEP Syndrome
- Periodic Paralysis (PP)
- Perlman Syndrome
- Pernicious Anemia
- Perrault Syndrome
- Pettigrew Syndrome
- Peutz-Jeghers Syndrome
- PHACE Syndrome
- Phenylketonuria
- Pheochromocytoma
- Phosphoenolpyruvate Carboxykinase Deficiency
- Phosphoglycerate Kinase Deficiency
- Phytosterolemia
- Pickwickian Syndrome
- Pierre Robin Syndrome
- Pilomatrixoma
- Pitt-Rogers-Danks Syndrome
- Pitt-Williams Brachydactyly Syndrome
- Pituitary Dwarfism
- Plott Syndrome
- Poland Syndrome
- Poland-Moebius Syndrome
- POLIP Syndrome
- Pollitt Syndrome
- Polyarteritis Nodosa (PAN)

- Polycystic Kidney Disease (PKD)
- Polycystic Liver Disease
- Polyostotic Osteolytic Dysplasia
- Porokeratosis of Mibelli
- Porphyrias
- Potter Syndrome
- Powell Venencie Gordon Syndrome
- Prader-Labhart-Willi Syndrome
- Precocious Puberty
- Primary Immunodeficiencies
- Primary Pulmonary Hypertension (PPH)
- Primary Torsion Dystonia
- Progeria Syndrome
- Progressive Bulbar Palsy of Childhood
- Progressive Familial Intrahepatic Cholestasis (PFIC)
- Prolidase Deficiency
- Propionic Acidemia
- Protein C Deficiency
- Protein S Deficiency
- Proteus Syndrome
- Proximal Muscular Dystrophy
- Prune Belly Syndrome
- Psaume Syndrome
- Pseudo-Achondroplastic Dysplasia
- Pseudohypoparathyroidism
- Pterygium Syndrome
- Pulmonary Alveolar Microlithiasis
- Pulmonary Alveolar Proteinosis
- Pulmonary Arteriovenous Malformation
- Pulmonary Hypoplasia
- Purine Nucleoside Phosphorylase Deficiency
- Purtscher Disease
- Pyknodysostosis
- Pyle Disease
- Pyruvate Carboxylase Deficiency
- Pyruvate Dehydrogenase Complex Deficiency
- Pyruvate Kinase Deficiency (PKD)