Orphanet J Rare Dis
Compound heterozygous IFT140 variants in two Polish families with Sensenbrenner syndrome and early onset end-stage renal disease.
Walczak-Sztulpa J, Posmyk R, Bukowska-Olech EM, Wawrocka A, Jamsheer A, Oud MM, Schmidts M, Arts HH, Latos-Bielenska A, Wasilewska A
Sensenbrenner syndrome, which is also known as cranioectodermal dysplasia (CED), is a rare, autosomal recessive ciliary chondrodysplasia characterized ...
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Source: PubMed
Dermatol Ther (Heidelb)
The Validity of Cutaneous Body Image as a Construct and as a Mediator of the Relationship Between Cutaneous Disease and Mental Health.
Hinkley SB, Holub SC, Menter A
Cutaneous body image (CBI) is a construct encompassing how individuals perceive their hair, skin, and nails. Negative CBI has been related to negative ...
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Source: PubMed
Imaging Sci Dent
Steatocystoma multiplex: A case report of a rare entity.
Shin NY, Kang JH, Kim JE, Symkhampa K, Huh KH, Yi WJ, Heo MS, Lee SS, Choi SC
Steatocystoma multiplex is an uncommon benign skin disease, which typically manifests as numerous intradermal cysts that can be scattered anywhere on ...
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Source: PubMed
Clin. Dermatol.
The color of skin: white diseases of the skin, nails, and mucosa.
Brown AE, Qiu CC, Drozd B, Sklover LR, Vickers CM, Hsu S
White diseases are a heterogenous group characterized by hypopigmentation or depigmentation. Skin and eye color are determined by the number and size ...
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Source: PubMed
Rev. Med. Virol. 2019 Dec 06
A review and meta-analysis of the epidemiology and clinical presentation of coxsackievirus A6 causing hand-foot-mouth disease in China and global implications.
Zhao TS, Du J, Sun DP, Zhu QR, Chen LY, Ye C, Wang S, Liu YQ, Cui F, Lu QB
Coxsackievirus A6 (CV-A6) has been associated with increasingly occurred sporadic hand-foot-mouth disease (HFMD) cases and outbreak events in many cou ...
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Source: PubMed
