कोरडी आणि खवलेयुक्त त्वचा यासारखे विविध जन्मजात रोग,

ichthyosis's Usage Examples:

Nonbullous congenital ichthyosiform erythroderma is a rare type of the ichthyosis family of skin diseases which occurs in 1 in 200,000 to 300,000 births.

Ichthyosis bullosa of Siemens is a type of familial, autosomal dominant ichthyosis, a rare skin disorder.

Hystrix-like ichthyosis–deafness syndrome (also known as "HID syndrome") is a cutaneous condition characterized by a keratoderma.

It is one of the notable aspects of newborns exhibiting congenital Harlequin-type ichthyosis, but ectropion can occur.

male had ichthyosis, hypogonadism, short stature, epilepsy, anemia, and polyneuritis.

For example, non-syndromic ichthyoses that are inherited recessively come under the umbrella term autosomal recessive congenital ichthyosis.

As such it is used to treat warts, calluses, psoriasis, dandruff, acne, ringworm, and ichthyosis.

Congenital ichthyosis[citation needed] Lamellar ichthyosis[citation needed] Harlequin type Ichthyosis[citation needed] Scarring.

IBIDS syndrome, following the acronym from ichthyosis, brittle hair and nails, intellectual impairment and short stature, is.

mutations in the gene encoding this protein have been associated with ichthyosis bullosa of Siemens.

As such, it is used to treat warts, psoriasis, acne vulgaris, ringworm, dandruff, and ichthyosis.

Epidermolytic ichthyosis (EI), also known as bullous epidermis ichthyosis (BEI), epidermolytic hyperkeratosis (EHK), bullous congenital ichthyosiform.

Keratitis–ichthyosis–deafness syndrome (also known as "Ichthyosiform erythroderma, corneal involvement, and deafness," and "KID syndrome,") presents at.