বিভিন্ন জন্মগত রোগ যা ত্বক শুষ্ক কোন ও আঁশযুক্ত একটি মাছের মত

ichthyosis's Usage Examples:

Harlequin-type ichthyosis is a genetic disorder that results in thickened skin over nearly the entire body at birth.

X-linked ichthyosis (abbreviated XLI) is a skin condition caused by the hereditary deficiency of the steroid sulfatase (STS) enzyme that affects 1 in 2000.

The more than 20 types of ichthyosis range in severity of.

Ichthyosis hystrix is a group of rare skin disorders in the ichthyosis family of skin disorders characterized by massive hyperkeratosis with an appearance.

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 vulgaris (also known as "Autosomal dominant ichthyosis," and "Ichthyosis simplex") is a skin disorder causing dry, scaly skin.

It is also known as Ichthyosis follicularis, alopecia, and photophobia syndrome or simply ichthyosis follicularis.

Ichthyosis acquisita is a disorder clinically and histologically similar to ichthyosis vulgaris.

The development of ichthyosis in adulthood can be a manifestation.

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

Lamellar ichthyosis, also known as ichthyosis lamellaris and nonbullous congenital ichthyosis, is a rare inherited skin disorder, affecting around 1 in.

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

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

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

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

skeletal abnormalities, distinguished by a sharp midline demarcation of the ichthyosis with minimal linear or segmental contralateral involvement.

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

Neonatal ichthyosis–sclerosing cholangitis syndrome (also known as "NISCH syndrome" and "ichthyosis–sclerosing cholangitis syndrome") is a cutaneous condition.

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

ichthyosis's Meaning':

any of several congenital diseases in which the skin is dry and scaly like a fish