ichthyosis उदाहरण वाक्य
उदाहरण वाक्य
- This means that a single mutation would cause a mild case of ichthyosis vulgaris and mutations to both copies of the gene would produce a more severe case.
- It is found largely in the upper spinous layer of epidermal keratinocytes and mutations in the gene encoding this protein have been associated with ichthyosis bullosa of Siemens.
- Individuals with truncation mutations in the gene coding for filaggrin are strongly predisposed to a severe form of dry skin, ichthyosis vulgaris, and / or eczema.
- Migratory lesions of ichthyosis linearis circumflexa may be caused by a dermal influx of inflammatory cells that undergo phagocytosis and digestion by keratinocytes, resulting in disruption of keratinization.
- It is one of the notable aspects of newborns exhibiting congenital Harlequin-type ichthyosis, but ectropion can occur due to any weakening of tissue of the lower eyelid.
- 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 ).
- 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 ).
- The disorder is related to CPDX2, and also has skin and skeletal abnormalities, distinguished by a sharp midline demarcation of the ichthyosis with minimal linear or segmental contralateral involvement.
- "' Zunich Kaye syndrome "', also known as "'Zunich neuroectodermal syndrome "', is a rare congenital ichthyosis first described in 1983.
- "' Ichthyosis hystrix "'is a group of rare skin disorders in the ichthyosis family of skin disorders characterized by massive hyperkeratosis with an appearance like spiny scales.