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- etimología
Qué (quién) es X-linked reticulate pigmentary disorder - definición
X-linked reticulate pigmentary disorder
RARE X-LINKED GENETIC CONDITION
Partington amyloidosis; Partington cutaneous amyloidosis; Reticulate pigmentary disorder; Familial cutaneous amyloidosis; Partington syndrome type II; X-linked reticulate pigmentary disorder with systemic manifestations
X-linked reticulate pigmentary disorder is a rare X-linked genetic condition in which males manifest multiple systemic symptoms and a reticulated mottled brown pigmentation of the skin, which, on biopsy, demonstrated dermal deposits of amyloid. Females usually only have linear streaks of hyperpigmentation.
X-linked dominant inheritance
MODE OF INHERITANCE
X-linked dominance; X-linked dominant
X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the X chromosome. As an inheritance pattern, it is less common than the X-linked recessive type.
X-linked intellectual disability
SYNDROMIC INTELLECTUAL CHARACTERIZED BY AN X-LINKED INHERITANCE PATTERN
X-Linked mental retardation; X-linked mental retardation
X-linked intellectual disability refers to medical disorders associated with X-linked recessive inheritance that result in intellectual disability.
