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A multidisciplinary approach is crucial for managing Silver-Russell syndrome effectively.

Catatonia can be a rare sign of lupus, needing careful diagnosis and treatment.

Early recognition of loose anagen hair syndrome is important to prevent misdiagnosis and unnecessary treatments.

Cicatricial pattern hair loss is likely advanced common baldness, not a type of lichen planopilaris.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Psychosis can be an early sign of neuropsychiatric lupus, treatable with tailored medication.

The woman's facial symptoms are best explained by primary Sjögren’s Syndrome.

A woman's hair loss was correctly diagnosed as Lichen planopilaris after initial misdiagnosis, highlighting the usefulness of trichoscopy in diagnosing hair disorders.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

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

Loose Anagen Syndrome is a hair condition where hairs can be easily pulled out, mainly affecting young girls, and may improve on its own or with treatment.

Frontal fibrosing alopecia may be linked to genital Lichen sclerosus through an autoimmune process.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

A Laotian man with unusual skin changes and multiple growths in his gut was diagnosed with Cronkhite-Canada Syndrome and improved with nutritional and immune-based treatments.

Lichen spinulosus, usually seen in young people, can rarely occur in adults, as shown by a 52-year-old woman with a rough, bumpy rash.

Chemical lumbar sympathectomy is an effective and safe treatment for idiopathic livedo reticularis.

The letter suggests that psychiatric issues, not a sleep disorder, were likely the cause of a patient's self-inflicted leg ulcers.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

The document concludes that a woman has both Frontal Fibrosing Alopecia and Lichen Simplex Chronicus, a previously unreported combination of conditions.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

The infant was diagnosed with Rothmund-Thomson syndrome, a rare genetic disorder causing various physical and developmental issues.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

A 4-year-old girl with a rare lupus condition was successfully treated with oral corticosteroids, leading to full recovery and hair regrowth.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Alopecia areata and lichen planus can occur together in children, which is important for diagnosis and treatment.

Lichen planus pigmentosus and fibrosing frontal alopecia in Colombia are likely different stages of the same disease.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.