Main description:

As clinical management of inherited metabolic diseases (IMDs) has improved, more patients affected by these conditions are surviving into adulthood. This trend, coupled with the widespread recognition that IMDs can present differently and for the first time during adulthood, makes the need for a working knowledge of these diseases more important than ever.

Inherited Metabolic Disease in Adults offers an authoritative clinical guide to the adult manifestations of these challenging and myriad conditions. These include both the classic pediatric-onset conditions and a number of new diseases that can manifest at any age. It is the first book to give a clear and concise overview of how this group of conditions affects adult patients, a that topic will become a growing imperative for physicians across primary and specialized care.

Contents:

PART A Metabolic pathways and their disorders in adults

Section 1 Disorders of carbohydrate metabolism
1 Glycogen Storage Disorders
David Cassiman, PascalLaforet, and Fanny Mochel
2 Galactosemia
Annet M. Bosch and Elaine Murphy
3 Disorders of fructose metabolism
Robin H. Lachmann and Timothy M. Cox.
4 Hyperinsulinemic hypoglycemia
Jean-Baptiste Arnoux and Pascal de Lonlay
5 Glut1 Deficiency
Joerg Klepper and Baerbel Leiendecker
Section 2 Disorders of mitochondrial energry metabolism
6 Pyruvate dehydrogenase complex deficiency
Mirian C.H. Janssen and Shamima Rahman
7 Disorders of mitochondrial energy metabolism
Shamima Rahman and Mirian C.H. Janssen
8 Fatty acid oxidation, electron transfer and riboflavin transport defects
Elaine Murphy, Christine Vianey-Saban, and Yann Nadjar
9 Disorders of ketogenesis and ketolysis
Andrew A. M. Morris
10 Disorders of creatine metabolism
David Cheillan and Frederuc Sedel
11 Coenzyme Q10 deficiency
Shamima Rahman and Mirian C.H. Janssen
Section 3 Disorders of protein metabolism
12 Phenylketonuria and Hyperphenylalaninaemia
Francjan J. van Spronsen and Robin H. Lachmann
13 Tyrosinaemia type I
David Cassiman and Wouter Meersseman
14 Tyrosinaemia type II
Elaine Murphy
15 Alkaptonuria
Wendy J. Introne
16 Branched Chain Amino Acids
Helen Prunty, Jamie L. Fraser, Charles P. Venditti, and Robin H. Lachmann
17 Urea Cycle Disorders
Stefan Koelker, Johannes Haberle and Valerie Walker
18 Citrin Deficiency
Adam H. Buchaklian and David P. Dimmock
19 Cystathionine beta-synthase deficiency or classical homocystinuria
Henk J Blom, Mirian C.H. Janssen, and Manuel Schiff
20 HHH syndrome
Carlo Dionisi-Vici, Diego Martinelli, Enrico Bertini, and Claude Bachmann
21 Glutaric aciduria type I
Stefan Koelker
22 2-hydroxyglutaric acidurias
Eduard A. Struys, Marjo S. van de Knaap, and Gajja S. Salomons
23 Serine Deficiency
Tom J. de Koning
24 Cystinuria
Aude Servais and Bertrand Knebelmann
25 Lysinuric Protein Intolerance & Hartnup Disease
Gianfranco Sebastio, Manuel Schiff, and Helene Ogier de Baulny
Section 4 Vitamin metabolism disorders
26 Biotinidase Deficiency and Biotin Holocarboxylase Synthetase Deficiency
Barry Wolf and Sara Elrefai
27 Disorders Of Cobalamin And Folate Metabolism
Jamie L. Fraser, Frederic Sedel, and Charles P. Vendetti
28 Disorders of thiamine metabolism
Frederic Sedel and Carla E. M. Hollak
Section 5 Neurotransmitters
29 Succinic Semialdehyde Dehydrogenase Deficiency
K. Michael Gibson, Cornelis Jakobs, and Philip L. Pearl
30 Atypical Nonketotic Hyperglycinemia
Argirios Dinopoulos
31 Biogenic monoamine disorders
Emmanuel Roze and Nenad Blau
32 Brain Serotonin Deficiency
Angels Garcia-Cazorla and Rafael Artuch Iriberri
Section 6 Dyslipidemias

33 Monogenic Chylomicronemia: Deficiency Of Lipoprotein Lipase And Related Factors
Amanda J. Brahm and Robert A. Hegele
34 Familial Lecithin Cholesterol Acyl Transferase Deficiency Syndromes
Dominic S. Ng
35 Tangier Disease
Dominic S. Ng
36 Familial Apolipoprotein A-I Deficiency
Dominic S. Ng
37 Abetalipoproteinemia And Hypobetalipoproteinemia
Amanda J. Hooper and John R. Burnett
Section 7 Cholesterol synthesis disorders

38 Smith-Lemli-Opitz Syndrome
Christopher Cunniff and Raoul C. Hennekam
39 Mevalonate kinase deficiency
Joost Frenkel and Hans R. Waterham
Section 8 Bile acid synthesis defects

40 Cerebrotendinous Xanthomatosis
Aad Verrips
41 Spastic paraplegia type 5
Fanny Mochel
Section 9 Disorders of purine and pyrimidine

42 Disorders of Purine Metabolism Affecting Adults
Irene Ceballos-Picot and H. A. Jinnah
Section 10 Porphyrias

43 Porphyrias
Janneke G. Langendonk and Timothy M. Cox
Section 11 Mineral and Metal Metabolism Disorders

44 Disorders of iron and copper metabolism
Jean-Marc Trocello and France Woimant
45 Disorders of Manganese Metablolism
Karin Tuschl, Peter T. Clayton, and Philippa B. Mills
Section 12 Lysosomal storage diseases

46 Lysosomal Storage Disorders
Ben Poorthuis
47 Gaucher Disease
Carla Hollak
48 Niemann-Pick disease type B
Tarekegn Geberhiwot and Carla E. M. Hollak
49 Fabry disease
Michael West and Gabor Linthorst
50 Gangliosidoses (GM1 and GM2)
Emmanuel Roze and Frederic Sedel
51 Krabbe disease in adults
Frederic Sedel
52 Metachromatic Leukodystrophy
Nicole Baumann and Jean-Claude Turpin
53 Niemann-Pick disease type C
Frederic Sedel
54 Mucopolysaccharidosis (MPS) in Adults
Christian J. Hendriksz and Francois Karstens
55 Pompe Disease
Ans T. van der Ploeg and Pascal Laforet
56 Danon Disease
Esther Brusse, Ans T van der Ploeg, Pascal Laforet
57 Oligosaccharidoses
Antonio Federico and Silvia Palmeri
58 Cholesteryl Ester Storage Disease
Carla E. M. Hollak
59 Neuronal Ceroid Lipofuscinoses
Catherine Caillaud and Frederic Sedel
60 Nephropathic cystinosis in adults
Aude Servais
Section 13 Peroxisomal disorders

61 X-Linked Adrenoleukodystrophy
Bjoern M. van Geel, Marc Engelen, and Stephan Kemp
62 Peroxisomal Disorders
Ronald J.A. Wanders and Hans R. Waterham
Section 14 Congenital Disorders of Glycosylation

63 Congenital disorders of glycosylation
Eva Morava and Mirian C.H. Janssen
Section 15 Miscellaneous

64 Trimethylaminuria
Robin H. Lachmann and Nigel Manning
65 Primary Hyperoxaluria
Jaap W. Groothoff
66 Disorders of complex lipids synthesis and remodeling
Foudil Lamari and Jean-Marie Saudubray

PART B Approach to the Patient

Section 1 Clinical Presentations

67 Neurological and Psychiatric symptoms
Frederic Sedel and Yann Nadjar
68 Chronic Fatigue and Acute Rhabdomyolysis
Ros Quinlivan and Pascal Laforet
69 Brain MRI In Inherited Metabolic Diseases Of Adulthood
Alessandro Burlina and Renzo Manara
70 Cardiac Aspects of IMDS
Perry Elliott and Giuseppe Limongelli
71 Approach To The Patient With Respiratory Signs And Symptoms
C.E.M. Hollak
72 Skeletal Abnormalities
Carla E.M. Hollak
73 Approach to the patient with general symptoms: fatigue and fever
Martijn C.G.J. Brouwers
74 Approach To The Patient With Hepato-Gastroenterological Or Abdominal Signs And Symptoms
David Cassiman and Carla E.M. Hollak
75 Ophthalmic manifestations of Inherited Metabolic Disease
Sarah Hull and Andrew R. Webster
76 Emergencies
Robin H. Lachmann and Elaine Murphy
77 Hematological Abnormalities
Carla E.M. Hollak
Section 2 Biochemical presentations

78 Hyperammonemia
Daniel Rabier
79 Approach To The Patient With Hyperhomocysteinaemia
Anthony Briddon
80 Hypoglycemia
Claire Douillard
81 Metabolic Acidosis
Steve Krywawych
82 Abnormalities of CSF neurotransmitters/ folates
Simon Heales, Simon Pope, Viruna Neergheen, and Manju Kurian

Part C Interpretation of some common specialist metabolic tests

83 Amino Acids
Daniel Rabier
84 Interpretation Of Organic Acid Analysis Results
Marinus Duran and Isabel Tavares de Almeida
85 Interpretation Of Acylcarnitine Analysis Results
Marinus Duran and Isabel Tavares de Almeida
86 Interpretation Of Very Long-Chain Fatty Acids Analysis Results
Frederic M. Vaz and Ronald J.A. Wanders

Part D Practical guidelines for the most prevalent disorders