TY - CHAP M1 - Book, Section TI - Gaucher Disease: Phenotypic and Genetic Variation A1 - Grabowski, Gregory A. A1 - Kolodny, Edwin H. A1 - Weinreb, Neal J. A1 - Rosenbloom, Barry E. A1 - Prakash-Cheng, Ainu A1 - Kaplan, Paige A1 - Charrow, Joel A1 - Pastores, Gregory M. A1 - Mistry, Pramod K. A2 - Valle, David L. A2 - Antonarakis, Stylianos A2 - Ballabio, Andrea A2 - Beaudet, Arthur L. A2 - Mitchell, Grant A. PY - 2019 T2 - The Online Metabolic and Molecular Bases of Inherited Disease AB - The marked phenotypic variation within and among the Gaucher disease clinical types has been known for several decades, but the characterization of this variation has generally been limited to relatively small patient populations (Sibille et al,148; Zimran et al,194; Zimran et al,191; Zimran et al,192). In addition, these characterizations are skewed because of the ascertainment bias in European-derived and, specifically, Ashkenazi Jewish populations. With broader knowledge about the major phenotypes, known as types 1, 2, and 3, the understanding of a spectrum or continuum has evolved with regard to clinical/pathologic involvement, particularly for the neuronopathic variants (Table 184-1; Fig. 184-1A). Excluding CNS involvement, the continuum extends to the variation in the visceral disease of overlapping involvement among and between type 1, 2, and 3 diseases (Fig. 184-1B). The advent of specific therapies for, the need for early prognostication in, and the search for modifying agents of Gaucher disease make complex phenotyping not merely an academic nosologic exercise, but of major practical and basic import. Thus, such distinctions impact whole-life medical care delivery, reproductive decisions, and therapeutic choices for affected families. Importantly, approaches to presymptomatic or prospective intervention therapies and/or use of therapies with significant risk require accurate risk-benefit analyses based on the prognosis for individual patients. Detailed phenotyping and correlations to genotype could provide insight into individual susceptibility to varying disease severity. This need represents a prime motivation to correlate phenotypes and genotypes in Gaucher disease as well as other inherited disorders. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/03 UR - ommbid.mhmedical.com/content.aspx?aid=1181465491 ER -