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Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Some new treatments for children's skin conditions are effective, but risks must be weighed.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

The most common skin condition at the Baqai Institute in Karachi was scabies, and eczema was the most prevalent group of diseases.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

A rare type of skin cancer with mucosal involvement was partially treated but eventually relapsed.

Retinoids might cause temporary hyperthyroidism in some patients.

The patient responded well to treatment with no disease progression.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

The document concludes that understanding tissue degeneration is crucial for diagnosing skin lesions.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

The man has a genetic skin condition called pachyonychia congenita.

PAON shows skin patterns due to genetic mosaicism.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

Loss of Desmocollin 3 in mice causes skin blisters and hair loss.

Fibroblasts are crucial for tissue repair and inflammation, and understanding them can help treat fibrotic diseases.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

Thyroid-related genes are active in skin cells and may affect autoimmune conditions.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Modulating Cytochrome P450 activity could help develop new skin disease treatments.

Early intervention and tailored management can reduce skin side effects from cancer treatments.

Vemurafenib causes skin side effects similar to RASopathies, requiring regular skin checks and UVA protection.

Follicular mucinosis can be an early sign of aggressive mycosis fungoides.

Keratin mutations cause skin diseases and could lead to new treatments.

Using your own skin cells can help repair aging skin and promote hair growth.