Clinical Molecular Science and Hereditary Diseases: Signaling, Diagnostic, and Management Contexts

£5.00

SKU: 9781738513413 Categories: , ,
Binding: Perfect Bound
Pages: 120Author: Dr. Muhammad Ramzan Manwar
 

Description

The current book is a research‑driven, distinctive resource that vividly explains the molecular aspects of hereditary disorders and reviews the dietary impact and management options grounded in preclinical and clinical literature. It also proposes how posttranslational modifications (e.g., glycosylation and phosphorylation) on membrane-bound proteins contribute to phenotypic heterogeneity observed in developmental disorders. Given the limited literature covering these facets, this mini-book will appeal to the enormous number of readers, including geneticists, pediatricians, pharmacists, chemists, healthcare professionals, dieticians, nutritionists, healthcare professionals, and medical students.

The author attempted to address below key questions:

  • How can non-invasive screening methods valuably help pediatric patients struggling with inherited disorders?
  • Can the combined charge and polarity of a mutant amino acid and nearby residues activate constitutive glycosylation and diverse phenotypic pathological outcomes in genetic disorders?
  • What non-canonical mechanisms can stimulate phenotypic variability, disease progression, and severity in developmental disorders?
  • How can glycan sequence and anomeric linkages inform the development of novel regimens for the management of hereditary diseases?
  • What lessons do multi-target therapeutic agents and combination therapies offer for treating or managing inborn disorders?
  • Do herbal compounds scavenge free radicals and provide adjunct antioxidant support that helps restore natural balance between oxidants and antioxidants in hereditary diseases, and to what extent?
  • Why is there a growing need to develop affordable, effective multi‑component therapeutic intervention models (nutritional, physical, educational, behavioral, therapeutic, digital, and electrical) to improve outcomes for patients with hereditary disorders?

This blend of disease signaling, screening, and management makes the book especially valuable to readers seeking descriptive ideas and practical, research‑informed future directions.

Additional information

Weight0.571 kg
Dimensions27.9 × 21.6 × 0.8 cm

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