Syndromes: Rapid Recognition and Perioperative Implications, 2e

Bruno Bissonnette, Igor Luginbuehl, Thomas Engelhardt

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• Aarskog Syndrome
• Aase Syndrome
• Aase-Smith Syndrome
• Abetalipoproteinemia
• Ablepharon-Macrostomia Syndrome (AMS)
• Acatalasia/Acatalasemia
• Achalasia-Alacrima Syndrome
• Achalasia-Microcephaly Syndrome
• Achard Syndrome
• Achard-Thiers Syndrome
• Acheiropodia
• Achondrogenesis
• Achondroplasia
• ACHOO Syndrome
• Ackerman Syndrome
• Acro-Fronto-Facio-Nasal Dysostosis Syndrome (Types I and II)
• Acro-Fronto-Facio-Nasal Dysostosis Syndrome Type I
• Acro-Fronto-Facio-Nasal Dysostosis Syndrome Type II
• Acrocephalopolysyndactylous Dysplasia
• Acrocephalopolysyndactyly Syndromes
• Acrocephalopolysyndactyly Type I: Noack Syndrome
• Acrocephalopolysyndactyly Type II: Carpenter Syndrome (CS)
• Acrocephalopolysyndactyly Type III: Sakati-Nyhan-Tisdale Syndrome
• Acrocephalopolysyndactyly Type IV: Goodman Syndrome
• Acrocephalosyndactyly Syndromes
• Acrocephalosyndactyly Type I: Apert Syndrome
• Acrocephalosyndactyly Type II: Crouzon Syndrome
• Acrocephalosyndactyly Syndrome Type III: Saethre-Chotzen Syndrome
• Acrocephalosyndactyly Type V: Pfeiffer Syndrome
• Acrodysostosis Syndrome
• Acrofacial Dysostosis: An Overview
• Acrofacial Dysostosis Nager Type
• Acrofacial Dysostosis Weyers Type
• Acrofacial Dysostosis Miller Type
• Acrofacial Dysostosis Lethal Type of Rodriguez (Acrofacial Dysostosis, Madrid Type)
• Acrofacial Dysostosis, Catania Type (Catania Brachydactylous Type of Acrofacial Dysostosis)
• Acrofacial Dysostosis, Palagonia Type (Palagonia Acrofacial Dysostosis)
• Acromesomelic Dysplasia
• Acromesomelic Dysplasia Type I: Maroteaux Type (AMDM)
• Acromicric Dysplasia
• Acrorenal-Mandibular Syndrome
• Acyl-CoA Dehydrogenase Deficiency Syndromes
• Short-chain Acyl-CoA Dehydrogenase Deficiency (SCADD)
• Medium-chain Acyl-CoA Dehydrogenase Deficiency (MCADD)
• Long-chain Acyl-CoA Dehydrogenase Deficiency (LCADD)
• Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHADD)
• Very-long-chain Acyl-CoA Dehydrogenase Deficiency (VLCADD)
• Multiple-chain Acyl-CoA Dehydrogenase Deficiency (MADD)
• Adactylia
• Adams-Nance Syndrome
• Adams-Oliver Syndrome (AOS)
• Addisonian Syndrome
• Adducted Thumbs Syndrome
• Adenosine Deaminase Deficiency

• Adie Syndrome (AS)
• Adrenogenital Syndrome
• Adrenomyodystrophy
• ADULT Syndrome
• AEC Syndrome
• Agnathia-Holoprosencephaly
• Aicardi Syndrome
• Aicardi-Goutières Syndrome (AGS)
• Ainhum
• Alacrima Congenita
• Alagille Syndrome (AS)
• Albinism
• Oculocutaneous Albinism (OCA)
• Oculocutaneous Albinism Type VIA: Hermansky-Pudlak Syndrome (HPS)
• Oculocutaneous Albinism Type VIB: Chediak-Higashi Syndrome (CHS)
• Albright Hereditary Osteodystrophy (AHO)
• Albright-Butler Syndrome
• Alexander Disease (AD)
• Alkaptonuria (AKU)
• Allan-Herndon-Dudley Syndrome (AHDS)
• Allgrove Syndrome
• Alopecia-Contractures-Dwarfism Mental Retardation Syndrome
• Alpers Syndrome
• Alpha₁-Antitrypsin Deficiency (AATD)
• Alpha-Ketoglutarate Dehydrogenase Deficiency
• Alpha-Mannosidosis
• Alport Syndrome (AS)
• Alström Syndrome
• Amelo-Onycho-Hypohidrotic Syndrome
• Amelogenesis Imperfecta (AI)
• Amenorrhea-Galactorrhea Syndrome (AGS)
• Amish Hair Brain Syndrome
• Amyotrophic Lateral Sclerosis
• Andermann Syndrome
• Andersen Cardiodysrhythmic Periodic Paralysis Syndrome
• Anderson-Tawil Syndrome (ATS)
• Angel-Shaped Phalangoepiphyseal Dysplasia (ASPED)
• Aniridia
• Ankyloblepharon Filiforme Adnatum and Cleft Palate
• Antley-Bixler Syndrome
• APECED Syndrome
• Aplasia Cutis Congenita (ACC)
• Apolipoprotein C-II Deficiency
• Argininemia
• Argininosuccinic Acid Lyase Deficiency (ASLD)
• Arkless-Graham Syndrome
• Arnold-Chiari Syndrome (ACS)
• Arrhythmogenic Right Ventricular Cardiomyopathy
• Arthrogryposis (Arthrogryposis Multiplex Congenita)
• Asymmetrical Short Stature Syndrome
• ATR-X Syndrome
• Atypical Mole Syndrome (AMS)
• Aughton Syndrome