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Infantile acropustulosis is an intensely itchy vesicopustular eruption of the hands and feet. [ 2 ] : 205 Involvement of scabies has been suggested. [ 3 ]
Gianotti-Crosti disease is a harmless and self-limiting condition, so no treatment may be required. [13] Treatment is mainly focused on controlling itching, symptomatic relief and to avoid any further complications. For symptomatic relief from itching, oral antihistamines or any soothing lotions like calamine lotion or zinc oxide may be used.
Acropustulosis refers to acrodermatitis with pustular involvement. Types include: Pustulosis palmaris et plantaris; Infantile acropustulosis; References.
Infantile acropustulosis (acropustulosis of infancy) Palmoplantar pustulosis (persistent palmoplantar pustulosis, pustular psoriasis of the Barber type, pustular psoriasis of the extremities, pustulosis of palms and soles, pustulosis palmaris et plantaris)
The non-infectious causes are generally benign and self-limited. [4] Erythema toxicum neonatorum; Transient neonatal pustular melanosis; Miliaria pustulosa; Infantile acropustulosis; Eosinophilic pustular folliculitis; Acne neonatorum (neonatal acne) Benign neonatal cephalic pustulosis (also called neonatal malasezzia furfur pustulosis)
BACM symptoms that follow are most frequently calf pain, gait complaints, and inability to walk. [2] The condition is self-limited and full restitution can be expected. In very rare cases, however, rhabdomyolysis may develop. [1] Affected are preschool and school-age children with a male predominance. [2]
Bobble-head doll syndrome is a rare neurological movement disorder in which patients, usually children around age 3, begin to bob their head and shoulders forward and back, or sometimes side-to-side, involuntarily, in a manner reminiscent of a bobblehead doll.
In rare situations, two normal parents can have a child with SCS due to a de novo mutation. The exact cause of the de novo mutation is unknown, but it doesn't seem to be related to anything that the parents did or didn't do during the pregnancy. [12] SCS due to a de novo mutation is so rare that the proportion of past cases is unknown. [7]