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The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

Men with a certain type of hair loss often use facial moisturizers, and a specific antibiotic treatment may help another hair condition.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Skin symptoms are important for diagnosing infections in children.

Tofacitinib may slow hair loss in scarring alopecias but is unlikely to regrow significant hair.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

An 11-year-old girl with Kawasaki disease experienced hair loss that improved after treatment.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

Treat pediatric skin issues with accurate diagnosis, multidisciplinary team, and various treatment options.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Breast cancer skin metastases are rare, look different, and can be confused with other skin issues, so a biopsy is needed for accurate diagnosis.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

The document concludes that accurate diagnosis of different types of hair loss requires careful examination of hair and scalp tissue, considering both clinical and microscopic features.

The document concludes that changes in eyelashes and eyelid skin can indicate various local and systemic diseases.

Trichoscopy is useful for diagnosing hair and scalp disorders in people with darker skin.

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

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Defects in certain proteins cause major heart abnormalities during early development.