1 citations
,
July 2022 in “BMJ Case Reports” A woman was wrongly diagnosed with lupus but actually had leprosy.
January 2025 in “Journal of Materials Chemistry B” July 2024 in “Journal of the American Academy of Dermatology” September 1996 in “Journal of the American Academy of Dermatology”
May 2000 in “Hair transplant forum international” The document's conclusion cannot be determined.
March 1998 in “Hair transplant forum international” The document could not be processed or understood.
May 1997 in “Hair transplant forum international” The document's conclusion cannot be summarized because the content is not accessible.
November 2024 in “JAAD Case Reports” A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.
1 citations
,
February 2006 in “The Journal of Urology” August 2006 in “The Journal of Urology”
November 2000 in “Hair transplant forum international” The document's conclusion cannot be provided because the content is not accessible.
April 2016 in “Annales de Dermatologie et de Vénéréologie” May 2025 in “Dermatology Reports” A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.
February 2026 in “Endokrynologia Polska” Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.
4 citations
,
March 2007 in “Hair transplant forum international” The document's conclusion cannot be provided as the content is not available.
9 citations
,
July 2010 in “British Journal of Dermatology” The document suggests a rare skin condition might be caused by a genetic phenomenon.
May 2018 in “International Society of Hair Restoration Surgery” March 2018 in “International Society of Hair Restoration Surgery” January 2018 in “International Society of Hair Restoration Surgery” September 2017 in “International Society of Hair Restoration Surgery” July 2017 in “International Society of Hair Restoration Surgery” May 2017 in “International Society of Hair Restoration Surgery”
1 citations
,
January 2023 in “Journal of Drugs in Dermatology” Early detection of Graham-Little-Piccardi-Lasseur syndrome is key for better management.
Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.
November 1995 in “Hair transplant forum international” The document cannot be understood or processed.
15 citations
,
October 2012 in “Journal of child neurology” The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.
September 2022 in “Zenodo (CERN European Organization for Nuclear Research)” MaasaLong may improve male health, but consult a doctor before use.
3 citations
,
February 2020 in “The Egyptian Rheumatologist” Recognizing LET and AITD can help diagnose SLE early for better treatment.
40 citations
,
January 2010 in “International Journal of Trichology” 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.