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- W2023599114 abstract "Under the caption Congenital Dyskeratosis, Erich Schafer1 described a syndrome based on observations gathered from one case of his own and from thirteen others reported in the literature. The condition is characterized by: pachyonychia; acneform, follicular keratosis, especially about the knees and elbows; symmetrical and circumscribed plantar and palmar keratosis; hyperhidrosis of the palms and soles; leukoplakia of the oral mucosa, and anomalies of the hair. All the fourteen cases showed pachyonychial changes as a constant finding, while the remaining clinical features were variants. In Schafer's case a boy, 12 years old, had had the characteristic ungual manifestations from birth. Brettauer's report2dealt with a boy 9 years old. The finger-nails were thickened, opaque, lusterless, partially loosened and in places swollen and lap-rolled in the longitudinal axis of the finger. According to Heller,1eJadassohn and Lewandowsky's case3of pachyonychia congenita belongs in this group. Siemens4likewise" @default.
- W2023599114 created "2016-06-24" @default.
- W2023599114 creator A5085948034 @default.
- W2023599114 date "1934-08-01" @default.
- W2023599114 modified "2023-09-27" @default.
- W2023599114 title "PACHYONYCHIA CONGENITA JADASSOHN" @default.
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- W2023599114 doi "https://doi.org/10.1001/archderm.1934.01460140044007" @default.
- W2023599114 hasPublicationYear "1934" @default.
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