• Source: Epidermolytic hyperkeratosis

Epidermolytic ichthyosis (EI), is a severe form of dry scaly skin, that initially presents with redness, blisters, erosions, and peeling in a newborn baby. Hyperkeratosis typically develops several months later. Other symptoms include itch, painful fissures, strong body odor, and absence of sweat. Symptoms vary in severity and extent of skin involvement. The two main types are divided into one involving palms and soles and the other without.
EI is caused by a genetic mutation. The condition involves the clumping of keratin filaments.
The condition is rare, affecting around 1 in 200,000 to 300,000 babies.




Signs and symptoms


EI is a severe form of dry scaly skin, that initially presents with redness, blisters, erosions, and peeling in a newborn baby. Hyperkeratosis typically develops several months later. Other symptoms include itch, painful fissures, body odor, and absence of sweat. Symptoms vary in severity and extent of skin involvement. Complications include infection and joint problems. Affected newborns are particularly at risk of dehydration, sepsis, and electrolyte imbalance.




Cause and mechanism


The condition is mostly inherited in an autosomal dominant pattern. To a lesser extent, a recessive form exists. It is caused by genetic mutations in the genes encoding the proteins keratin 1 or keratin 10, resulting in disruption of the structure of the epidermis.

Keratin 1 is associated with the variants affecting the palms and soles.
Keratin 10 is associated with the variants in which these are unaffected.




Diagnosis


Diagnosis is by its appearance, skin biopsy, and genetic testing.
The condition can be diagnosed via exam that reveals; generalized redness; thick, generally dark, scales that tend to form parallel rows of spines or ridges, especially near large joints; the skin is fragile and blisters easily following trauma; extent of blistering and amount of scale is variable.




Treatment


Treatment includes applying thick moisturisers. Other therapies include topical and oral retinoids. These include topical N-acetylcysteine, liarozole, and calcipotriol. Bacterial colonisation of skin may be reduced by use of antibacterial soaps, chlorhexidine, and dilute sodium hypochlorite baths.




Research


Gene therapy is being studied for EI.




Epidemiology


The condition is rare, affecting around 1 in 200,000 to 300,000 babies.




History


EI was first classified by its presence or absence in the palms and soles by DiGiovanna and Bale in 1994.




See also


Ichthyosis bullosa of Siemens
Isotretinoin (Accutane)
List of cutaneous conditions
List of cutaneous conditions caused by mutations in keratins
List of verrucous carcinoma subtypes
Nonbullous ichthyosiform erythroderma




Notes






References






External links

Kata Kunci Pencarian:

• Epidermolytic hyperkeratosis
• Hyperkeratosis
• Keratin 10
• Palmoplantar keratoderma
• Epidermolytic acanthoma
• Howel–Evans syndrome
• List of skin conditions
• Ichthyosis hystrix
• Genodermatosis
• Killer Croc