Physician's Guide to the Laboratory Diagnosis of Metabolic Diseases

N. Blau, M. Duran, M.E. Blaskovics, K.M. Gibson (Herausgeber)

Media-Kombination

XXXVII, 716 Seiten

2002 | 2., nd ed. 2002. Corr. 2nd printing 2004
Springer Berlin
978-3-540-42542-7 (ISBN)

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Delay and mistakes in the diagnosis of inherited metabolic diseases may have devastating consequences. Reference laboratory data are scattered and clinical descriptions of rare conditions are hard to locate. This book describes 298 disorders, grouped into 35 chapters according to the type of condition. Within each group of disorders, chapters provide tables of pertinent clinical findings as well as reference and pathological values for crucial metabolites. Relevant metabolic pathways and diagnostic flow charts are included. There are four indices to make the book as user-friendly as possible: Disorders index, Signs and symptoms index, Organs index, and Tests index. The Physician's Guide provides paediatricians and other physicians with a unique aid to help them select the correct diagnosis from a bewildering array of complex clinical and laboratory data.
Systemvoraussetzungen PC:
Pentium, Windows 95 OSR 2.0/98 SE/Me/NT 4.0 with Service Pack 5/2000/XP, 64 MB of RAM, 24 MB of available hard-disk space.
Systemvoraussetzungen Macintosh:
Power PC, System 8.6/9.0.4/9.1/OS, 64 MB of RAM, 24 MB of available hard-disk space.

The program also runs under UNIX computers when the free Adobe Acrobat Reader is installed.

From the contents:
- Diagnosis
- Simple tests; Amino acid analysis; Organic acid analysis ; Miscellaneous analyses; Tandem mass spectrometry; Proton NMR spectroscopy. Disorders
- Phenylalanine, tetrahydrobiopterin metabolism; Neurotransmitter metabolism; GABA, serine, glycine, prolin; Tyrosinemias; Histidine metabolism; Leucine metabolism; Isoleucine-valine metabolism; Organic acidurias; Gamma-glutamyl cycle; Sulfur amino acids; Inherited hyperamonemias; Ornitine, lysine, tryptopha; Defective transport of amino acids; Fatty acids beta-oxidation; Carbohydrates, glycogen disorders; Glucose transport; Glycerol metabolism; Mucopolysaccharidoses; Oligosaccharidoses, related disorders; Congenital disorders glycosylation; Cystinosis; Storage disorders; Purine, pyrimidine; Creatine synthesis, transport defects; Peroxisomal disorders; Hyperoxalurias; Mitochondrial disorders; Genetic dyslipoproteinemias; Steroid synthesis, metabolism; Inborn errors cholesterol biosynthes is; Porphyrias; Bile acidsynthesis; Cu, Zn, Fe metabolism; Leukotrienes

Vorwort	C.R. Scriver
Sprache	englisch
Maße	193 x 242 mm
Gewicht	1558 g
Themenwelt	Naturwissenschaften ► Biologie ► Biochemie
Schlagworte	Biochemie; Handbuch/Lehrbuch • Genetics • inborn errors • laboratory tests • Labormedizin; Handbuch/Lehrbuch • Metabolic disorders • Stoffwechselkrankheiten
ISBN-10	3-540-42542-X / 354042542X
ISBN-13	978-3-540-42542-7 / 9783540425427
Zustand	Neuware