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Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

A 4-year-old girl has a rare hair condition causing fragile, short hair.

ODC transgenic mice can model human hair loss with skin lesions.

A rare, non-cancerous ovarian tumor was successfully treated with surgery, improving the patient's symptoms.

Halo Scalp Ring is a rare newborn hair loss that can be missed, and early diagnosis can avoid extra tests and worry for parents.

New method, hair distribution width (HDW), improves accuracy in diagnosing androgenetic alopecia (AGA).

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

Early diagnosis of imperforate hymen is crucial to prevent complications.

Women with hyperandrogenism, especially those with PCOS, are more likely to have psychiatric disorders.

Idiopathic hirsutism is the most common cause of hirsutism in women, followed by PCOS.

Trichofolliculoma was found in a person with amniotic band syndrome for the first time.

Children with vitiligo may have other health issues like skin, thyroid, and mental health problems.

About 13% of women had idiopathic hirsutism and 8.5% had polycystic ovary syndrome in a group of Iranian women.

Hormonal therapy is essential in late-diagnosed Kallmann's syndrome to prevent bone issues.

Early recognition and treatment of VATS in transplant patients improve outcomes.

Robertsonian translocation can cause recurrent miscarriages.

The research found that polycystic ovary syndrome (PCOS) has two distinct types, with one having more severe hormone and insulin issues.

An infant had two different natural hair colors on the scalp with no health issues.

Asian women often experience distinct hair thinning at the top of the head.

A 54-year-old woman experienced progressive hair loss starting in adolescence, leading to sparse scalp hair and almost no eyebrows or eyelashes.

Diagnosing Sertoli-Leydig cell tumors is challenging due to their unusual symptoms and can occur at any age.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Temporal triangular alopecia may be linked to sebaceous nevus and shows a new pinkish background feature.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

PCOS phenotypes A and B are more common and linked to higher health risks in women from the Ecuadorian Andes.

Basal cell carcinoma may originate from vellus hair cysts.