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Yunis-Varon syndrome: further delineation of the phenotype.
Basel-Vanagaite L, Kornreich L, Schiller O, Yacobovich J, Merlob P. Basel-Vanagaite L, et al. Am J Med Genet A. 2008 Feb 15;146A(4):532-7. doi: 10.1002/ajmg.a.32135. Am J Med Genet A. 2008. PMID: 18203163 Review.
Yunis-Varon syndrome (YVS) is a rare autosomal recessive condition characterized by limb defects, ossification defects, generalized hypotrichosis and, frequently, a severe neonatal course. The molecular basis is unknown. We report on a newborn infant with previously undesc …
Yunis-Varon syndrome (YVS) is a rare autosomal recessive condition characterized by limb defects, ossification defects, generalized hypotric …
Clouston Syndrome: 25-year follow-up of a patient.
Trídico LA, Antonio JR, Pozetti EM, Rosa AM, Antonio CR. Trídico LA, et al. An Bras Dermatol. 2015 Nov-Dec;90(6):897-9. doi: 10.1590/abd1806-4841.20153990. An Bras Dermatol. 2015. PMID: 26734875 Free PMC article.
This paper reports a 25-year follow-up of a patient with Clouston syndrome, from childhood to adulthood, monitoring diagnosis and clinical course of the disease....
This paper reports a 25-year follow-up of a patient with Clouston syndrome, from childhood to adulthood, monitoring diagnosis and clinical …