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Image of - Physicians Guide To The Diagnosis Treatment And Follow Up Of Inherited Metabolic Diseases 2nd Edition | Hardcover
Physicians Guide To The Diagnosis Treatment And Follow Up Of Inherited Metabolic Diseases 2nd Edition | Hardcover

Physicians Guide To The Diagnosis Treatment And Follow Up Of Inherited Metabolic Diseases 2nd Edition | Hardcover

by Blau N.

This updated and enlarged second edition is a unique source of information on the diagnosis, treatment, and follow-up of metabolic diseases. The clinical and laboratory data characteristic of rare metabolic conditions can be bewildering for clinicians and laboratory personnel alike “ reference laboratory data is scattered, and clinical descriptions can be obscure. The new Physicians Guide with the additional more than 600 diseases now featured, documents 1200 conditions grouped according to type of disorder, organ system affected (e.g. liver, kidney, etc) or phenotype (e.g. neurological, hepatic, etc). It includes relevant clinical findings and highlights the pathological values for diagnostic metabolites. Guidance on appropriate biochemical genetic testing is also provided and established experimental therapeutic protocols are described, with recommendations on follow-up and monitoring. The authors are acknowledged experts, and the book is a valuable desk reference for all who deal with inherited metabolic diseases.

Highlights

  • binding-icon

    9783030677268

    ISBN:

  • binding-icon

    Blau N.

    Author:

  • binding-icon

    1534

    Pages:

  • binding-icon

    4710 gm

    Weight:

  • langauage-icon

    English

    Language:

  • date-icon

    2022

    Year:

  • edition-icon

    2nd Edition

    Edition:

  • binding-icon

    Hardcover

    Binding:

₹18592

₹23240

This updated and enlarged second edition is a unique source of information on the diagnosis, treatment, and follow-up of metabolic diseases. The clinical and laboratory data characteristic of rare metabolic conditions can be bewildering for clinicians and laboratory personnel alike “ reference laboratory data is scattered, and clinical descriptions can be obscure. The new Physicians Guide with the additional more than 600 diseases now featured, documents 1200 conditions grouped according to type of disorder, organ system affected (e.g. liver, kidney, etc) or phenotype (e.g. neurological, hepatic, etc). It includes relevant clinical findings and highlights the pathological values for diagnostic metabolites. Guidance on appropriate biochemical genetic testing is also provided and established experimental therapeutic protocols are described, with recommendations on follow-up and monitoring. The authors are acknowledged experts, and the book is a valuable desk reference for all who deal with inherited metabolic diseases.

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