ichthyosiform การใช้

Children who survive the neonatal period usually evolve to a less severe phenotype, resembling a severe congenital ichthyosiform erythroderma.
Ichthyosiform sarcoidosis is a cutaneous condition resembling ichthyosis vulgaris or acquired ichthyosis, with fine scaling usually on the distal extremities, by caused by sarcoidosis.
Most cases ( approximately 75 % ) of collodion baby will go on to develop a type of autosomal recessive congenital ichthyosis ( either lamellar ichthyosis or congenital ichthyosiform erythrodema ).
"' Congenital hemidysplasia with ichthyosiform erythroderma and limb defects "'( also known as " CHILD syndrome " ) is a genetic disorder with onset at birth seen almost exclusively in females.
It is also referred to as "'CHIME syndrome "', after its main symptoms ( colobomas, heart defects, ichthyosiform dermatosis, intellectual disability, and either ear defects or epilepsy ).