Introduction to Hereditary Skin

Sentence Examples

Discover more insights into Hereditary Skin

Keywords frequently search together with Hereditary Skin

Narrow sentence examples with built-in keyword filters

Hereditary Skin sentence examples within hereditary skin disease

hereditary skin disease

Ichthyosis is an extensive group of hereditary skin diseases characterized by keratinization disorders of the type of hyperkeratosis, which leads to the formation of scales on the skin resembling fish scales.

On epidemiology of congenital ichthyosis in Moscow

hereditary skin disease

Non-viral gene therapy for hereditary skin diseases is an attractive prospect.

Highly Branched Poly(β-amino ester)s for Gene Delivery in Hereditary Skin Diseases.

More hereditary skin disease sentences More Sentences

Hereditary Skin sentence examples within hereditary skin disorder

hereditary skin disorder

Intrinsic factors include factors such as advanced age, immune compromise, psychological stress, hereditary skin disorders, and disease states/comorbidities.

Wound management.

hereditary skin disorder

The importance of G12 substitutions in these beta-connexins is revealed in two hereditary skin disorders, keratitis ichthyosis and erythrokeratodermia variabilis, both of which result from missense mutations affecting G12.

The Complex and Critical Role of Glycine 12 (G12) in Beta-Connexins of Human Skin

More hereditary skin disorder sentences More Sentences

More Hereditary Skin sentence examples
10.1590/FST.39720

Facial greenish brown birthmark, also known as zygomatic mother spot and acquired bilateral nevoid spot of Ota, is a congenital non hereditary skin pigmentation disease, mainly distributed symmetrically on both sides of zygoma, involving forehead, temporal, periocular and alar nose, pigmentation on the dermis, showing round or oval cyan or light brown patches, with clear edge and mutual fusion of adjacent lesions (Hui et al.

Effect of turning-Q laser in combination with topical Chuangfukang collagen mask to improve facial appearance, greenish brown birthmark area and color depth of patients with facial greenish brown birthmark

More Hereditary Skin sentence examples
10.33667/2078-5631-2021-18-59-62

Ichthyosis is an extensive group of hereditary skin diseases characterized by keratinization disorders of the type of hyperkeratosis, which leads to the formation of scales on the skin resembling fish scales.

On epidemiology of congenital ichthyosis in Moscow

More Hereditary Skin sentence examples
10.1016/j.addr.2021.113842

Non-viral gene therapy for hereditary skin diseases is an attractive prospect.

Highly Branched Poly(β-amino ester)s for Gene Delivery in Hereditary Skin Diseases.

More Hereditary Skin sentence examples
10.14701/ahbps.NURSE-SY-1-1

Intrinsic factors include factors such as advanced age, immune compromise, psychological stress, hereditary skin disorders, and disease states/comorbidities.

Wound management.

More Hereditary Skin sentence examples
10.1016/j.scr.2021.102213

Netherton syndrome (NS) is a rare, autosomal recessive hereditary skin disease caused by mutations in SPINK5 gene, characterized with severe skin barrier damage.

Establishment of an induced pluripotent stem cell line (SAHGMUi001-A) from a patient with Netherton syndrome carrying SPINK5 mutation.

More Hereditary Skin sentence examples
10.3390/ijms22052615

The importance of G12 substitutions in these beta-connexins is revealed in two hereditary skin disorders, keratitis ichthyosis and erythrokeratodermia variabilis, both of which result from missense mutations affecting G12.

The Complex and Critical Role of Glycine 12 (G12) in Beta-Connexins of Human Skin

More Hereditary Skin sentence examples
10.1186/s12920-020-00851-5

Background Familial progressive hyper- and hypopigmentation (FPHH, MIM 145250) is a rare hereditary skin disorder that is predominantly characterized by progressive, diffuse, partly blotchy hyperpigmented lesions intermingled with scattered hypopigmented spots, lentigines and sometimes Cafe-au-lait spots (CALs).

Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation

More Hereditary Skin sentence examples
10.1111/jdv.17524

Non‐syndromic congenital ichthyosis describes a heterogeneous group of hereditary skin disorders associated with erythroderma and scaling at birth.

High rate of self‐improving phenotypes in children with non‐syndromic congenital ichthyosis: case series from south‐western Germany

More Hereditary Skin sentence examples
10.5772/intechopen.97036

Epidermolysis bullosa (EB) is a group of hereditary skin diseases, or genodermatoses, characterized by the formation of severe, chronic blisters with painful and life-threatening complications.

Surgical Treatment of Wounds Using Stem Cells in Epidermolysis Bullosa (EB)

More Hereditary Skin sentence examples
10.5582/IRDR.2020.03150

In limited-resource settings such as Indonesia, diagnoses of hereditary skin disease often rely on clinical features.

Novel mutations of epidermolysis bullosa identified using whole-exome sequencing in Indonesian Javanese patients.

Learn more from Hereditary Skin

Keywords related to Hereditary

Hereditary Skin
Encyclopedia

What is/are Hereditary Skin?

Hereditary Skin - Facial greenish brown birthmark, also known as zygomatic mother spot and acquired bilateral nevoid spot of Ota, is a congenital non hereditary skin pigmentation disease, mainly distributed symmetrically on both sides of zygoma, involving forehead, temporal, periocular and alar nose, pigmentation on the dermis, showing round or oval cyan or light brown patches, with clear edge and mutual fusion of adjacent lesions (Hui et al. [1] Ichthyosis is an extensive group of hereditary skin diseases characterized by keratinization disorders of the type of hyperkeratosis, which leads to the formation of scales on the skin resembling fish scales. [2] Non-viral gene therapy for hereditary skin diseases is an attractive prospect. [3] Intrinsic factors include factors such as advanced age, immune compromise, psychological stress, hereditary skin disorders, and disease states/comorbidities. [4] Netherton syndrome (NS) is a rare, autosomal recessive hereditary skin disease caused by mutations in SPINK5 gene, characterized with severe skin barrier damage. [5] The importance of G12 substitutions in these beta-connexins is revealed in two hereditary skin disorders, keratitis ichthyosis and erythrokeratodermia variabilis, both of which result from missense mutations affecting G12. [6] Background Familial progressive hyper- and hypopigmentation (FPHH, MIM 145250) is a rare hereditary skin disorder that is predominantly characterized by progressive, diffuse, partly blotchy hyperpigmented lesions intermingled with scattered hypopigmented spots, lentigines and sometimes Cafe-au-lait spots (CALs). [7] Non‐syndromic congenital ichthyosis describes a heterogeneous group of hereditary skin disorders associated with erythroderma and scaling at birth. [8] Epidermolysis bullosa (EB) is a group of hereditary skin diseases, or genodermatoses, characterized by the formation of severe, chronic blisters with painful and life-threatening complications. [9] In limited-resource settings such as Indonesia, diagnoses of hereditary skin disease often rely on clinical features. [10]

hereditary skin disease

Ichthyosis is an extensive group of hereditary skin diseases characterized by keratinization disorders of the type of hyperkeratosis, which leads to the formation of scales on the skin resembling fish scales. [1] Non-viral gene therapy for hereditary skin diseases is an attractive prospect. [2] Netherton syndrome (NS) is a rare, autosomal recessive hereditary skin disease caused by mutations in SPINK5 gene, characterized with severe skin barrier damage. [3] Epidermolysis bullosa (EB) is a group of hereditary skin diseases, or genodermatoses, characterized by the formation of severe, chronic blisters with painful and life-threatening complications. [4] In limited-resource settings such as Indonesia, diagnoses of hereditary skin disease often rely on clinical features. [5]

hereditary skin disorder

Intrinsic factors include factors such as advanced age, immune compromise, psychological stress, hereditary skin disorders, and disease states/comorbidities. [1] The importance of G12 substitutions in these beta-connexins is revealed in two hereditary skin disorders, keratitis ichthyosis and erythrokeratodermia variabilis, both of which result from missense mutations affecting G12. [2] Background Familial progressive hyper- and hypopigmentation (FPHH, MIM 145250) is a rare hereditary skin disorder that is predominantly characterized by progressive, diffuse, partly blotchy hyperpigmented lesions intermingled with scattered hypopigmented spots, lentigines and sometimes Cafe-au-lait spots (CALs). [3] Non‐syndromic congenital ichthyosis describes a heterogeneous group of hereditary skin disorders associated with erythroderma and scaling at birth. [4]