Harlequin Baby

Harlequin Baby. Harlequin ichthyosis is a severe inherited form of ichthyosis that presents at birth as hard thickened armourlike plates of skin covering the entire body Harlequin ichthyosis is also called harlequintype ichthyosis and harlequin fetus [1].

Harlequin color change is a cutaneous condition seen in newborn babies characterized by momentary red color changes of half the child sharply demarcated at the body’s midline This transient change occurs in approximately 10% of healthy newborns It is seen usually between two and five days of birth.

What causes harlequin baby syndrome? – JanetPanic.com

What is Harlequin baby? Harlequin ichthyosis is a severe genetic disorder that mainly affects the skin The newborn infant is covered with plates of thick skin that crack and split apart The thick plates can pull at and distort facial features and can restrict breathing and eating Mutations in the ABCA12 gene cause harlequin ichthyosis.

Harlequin syndrome Genetic and Rare Diseases …

Harlequin syndrome is a syndrome affecting the autonomic nervous system [1] The autonomic nervous system is responsible for controlling the body’s natural processes such as sweating skin flushing and the response of the pupils to stimuli [2] People with Harlequin syndrome have the absence of sweating and flushing of skin on one side of the body.

Harlequin Ichthyosis Baby – New Indian Journal of Pediatrics

Harlequin colour change appears transiently in approximately 10% of healthy newborns1This distinctive phenomenon presents as a welldemarcated colour change with one half of the body displaying erythema and the other half pallor Usually occurring between two and five days of age harlequin colour change has been seen as late as three weeks of age2The.