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THA is a rare condition with no significant clinical consequences if thyroid function is normal.

A woman's severe male hormone excess was caused by a small, hard-to-find ovarian tumor.

The family has a unique form of ectodermal dysplasia similar to Clouston syndrome but with different hair and skin symptoms.

Skin issues from chronic graft-versus-host disease greatly affect daily life, needing teamwork between blood and skin doctors.

Hirsutism in teen girls is common, usually harmless, but can sometimes signal serious issues and is treatable.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

A 23-year-old woman's missed periods were caused by a rare genetic disorder treated with hormone patches.

South Asian women with PCOS experience more psychological distress and have a poorer quality of life, especially in social relationships, with hirsutism affecting them more than obesity.

Treatment restored normal sexual characteristics and blood condition in a patient with testicular cancer.

The 6-year-old Somalian girl fully recovered from her symptoms after successful surgery and treatment.

Hirsutism in women is mostly due to PCOS and can be managed with oral contraceptives and hair removal methods.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Bullous pemphigoid, intrahepatic cholangiocarcinoma, and alopecia areata may share immune-related causes.

Hidradenitis suppurativa is a chronic skin condition causing painful lumps and scarring, often triggered by smoking and obesity, and requires varying treatments based on severity.

High beta-hydroxybutyrate levels may worsen hair loss in alopecia areata.

Women with more body hair tend to have thicker belly fat and more metabolic health issues.

Managing rare genetic diseases like osteogenesis imperfecta and Escobar syndrome is complex and requires both medical and surgical treatments.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Early diagnosis and treatment of Kaposi varicelliform eruption are crucial to prevent severe complications.

A patient with Satoyoshi syndrome improved with a treatment combining several medications, including carbamazepine and methotrexate.

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

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

Hidradenitis suppurativa is likely caused by blocked hair follicles, not apocrine glands.

A young woman's symptoms suggested PCOS, but tests and surgery confirmed and treated a rare ovarian tumor, resolving her condition.

Neuroendocrine paraneoplastic syndromes often show skin changes, helping early diagnosis and requiring a team approach for best care.

Biotin improved hair growth and combability in one child with uncombable hair syndrome.

People with chronic hives should be tested for thyroid autoimmunity to manage their condition better.

Polycystic Ovary Syndrome (PCOS) is common in women with conditions like anovulation, hirsutism, hair loss, and type 2 diabetes, and it can lead to health risks like heart disease, obesity, insulin resistance, and depression. Non-Classic Congenital Adrenal Hyperplasia (NC-CAH) is also discussed.

A man's skin condition was misdiagnosed and later identified as a rare type of skin cancer, which did not improve with treatment.

The patient with EEC syndrome had scarring alopecia due to deep folliculitis, possibly linked to abnormal hair structure.