Recognition of rare chromosomal disorders remains particularly important in populations that are underrepresented in the medical literature. This book presents the first documented Iraqi case of Jean de Grouchy syndrome, also known as 18p deletion syndrome or partial monosomy 18p. Beyond describing an individual patient, the book places the case within the historical evolution of 18p deletion syndrome, from its original recognition in 1963 through subsequent reports that established its broad and variable clinical spectrum. It illustrates the enduring value of careful clinical observation, phenotypic documentation, cytogenetic investigation, and publication in expanding recognition of rare chromosomal disorders and enriching the medical literature with previously underrepresented Iraqi clinical experience.
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