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UVA1-light therapy successfully treated a child's skin condition, mycosis fungoides.

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

The book details skin conditions in older adults, their link to mental health, cancer treatment importance, hair loss remedies, and managing autoimmune and itchy skin.

Alopecia areata in infants may be more common than previously thought.

Finasteride use may cause sexual dysfunction; more research needed.

Gynecologists should provide comprehensive care for transgender patients, including mental health evaluation, hormone therapy, and surgical options, while monitoring for side effects and ensuring patient safety.

Male pattern baldness may be caused by factors like poor blood circulation, scalp tension, stress, and hormonal imbalances, but the exact causes are still unclear.

Hormones significantly affect women's sexual function, and more research is needed to improve treatments for sexual dysfunction with minimal side effects.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

The surgery for severe congenital ptosis in children is safe and effective, with good long-term results.

Minoxidil use during pregnancy can cause excessive hair growth and multiple birth defects in the baby.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

Congenital alopecia in domestic animals is rare and involves abnormal hair follicle development, needing better understanding and classification.

Some babies are born with alopecia areata, and a treatment with clobetasol propionate can regrow hair in half of the cases.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Lash ptosis is more common and severe in people with congenital eyelid droop than in those with acquired eyelid droop or without eyelid droop.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

The modified Crawford technique resulted in less lagophthalmos and better cosmetic outcomes for patients with lateral droop.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.