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Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

The document discusses a young boy with autism and early puberty but does not provide a conclusion on managing his behavior.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Unmarried women with PCOS in Pakistan face stigma and use various strategies to cope, needing better support and accurate information.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

Acne is strongly linked to high BMI, hair loss, menstrual issues, family history, and eating too many sweets and fatty foods, but not to excessive hair growth.

Cronkhite-Canada syndrome is a rare condition causing gut polyps, hair loss, skin changes, and nail issues, often with a poor outlook.

Children with alopecia areata often face neglectful parenting, leading to higher anxiety and depression.

Most hair disorder patients at the clinic were young adult males, with alopecia areata being the most common condition.

PCOS and related metabolic issues often run in families.

Hair loss from alopecia areata can sometimes regrow in a pattern similar to androgenetic alopecia.

Lichen Planus in siblings may be influenced by genetics and environment.

Male relatives of women with PCOS show similar health issues, suggesting a male version of the condition.

Young men with scalp psoriasis and hair loss fears may develop compulsive scalp behaviors needing attention.

Lichen planopilaris may have a genetic link.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

Many in Saudi Arabia experience early hair loss but lack awareness of treatments.

Nail changes in alopecia areata are common and may indicate severity and genetic risk.

Timely treatments like PRP, topical, and drugs can effectively reduce hair loss.

Children with alopecia areata often experience more anxiety and depression, linked to neglectful family dynamics.

Using animal names for skin conditions helps with learning and memory.

Minoxidil, a common hair treatment, may cause hair to turn grey or change color, especially with long-term use or if you have a family history of grey hair.

Hirsutism is common among Iraqi women, often without a known cause, but family history is significant.

A rare skin condition in a 17-year-old was diagnosed late, stressing the need for careful evaluation and genetic testing.

Three genes linked to the development of trichilemmal cysts were found.

The grey patch variant of tinea capitis is most common, mainly spread through family and animals.

Frontal fibrosing alopecia and ulerythema ophryogenes may be related and can evolve from one to the other.

Hair loss from chemotherapy causes significant distress and affects social roles for ovarian and uterine cancer patients.

A rare skin condition called Eruptive Vellus Hair Cyst can cause itchy papules on the face.