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A cat in Turkey had Ehlers-Danlos syndrome, showing very stretchy skin and easy bruising.

A 19-month-old Saudi girl had a rare skin condition with no other defects, and her family was unaffected.

Recognizing the "bamboo hair defect" is crucial for diagnosing Netherton's syndrome.

Plet-1 protein helps hair follicle cells move and stick to tissues.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.

Recognizing and treating skin symptoms in essential thrombocythemia is crucial for patient quality of life.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Panitumumab can cause excessive ear hair growth.

A young boy's uncombable hair is due to a rare genetic condition that usually improves over time.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

Diagnosing and managing monilethrix is harder when it occurs with other hair loss conditions.

Diagnosing and managing monilethrix is harder when it occurs with other hair loss conditions.

Thymoma may link myasthenia gravis, nail dystrophy, and alopecia areata.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

A rare finger tumor was imaged, showing a unique pattern not seen before.

Thymic epithelial cells may be related to skin stem cells.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Mice with more Flightless I protein grew back their claws better after amputation.

Trichotillomania is a condition where people repeatedly pull out their hair, which can be triggered by stress and has various physical signs.

Monotreme hair structure and protein distribution are similar to other mammals, but their inner root sheath cornifies differently, suggesting a unique evolution from reptile skin.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

Plica polonica is a rare condition where hair becomes irreversibly tangled, and the treatment is to cut the matted hair.