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tricho·dys·tro·phy (trik″o-disґtrə-fe) any disorder of the hair marked by defects in the structure of the hair shaft, frequently manifested by alopecia with lusterless, fractured hair.Medical dictionary. 2011.
Tay syndrome — Infobox Disease Name = Tay syndrome Caption = DiseasesDB = 13341 ICD10 = ICD9 = ICDO = OMIM = 601675 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Tay syndrome is a recessive hereditary disease characterised by trichothiodystrophy… … Wikipedia
monilethrix — An autosomal dominant trichodystrophy in which brittle hairs show a series of constrictions, usually without a medulla. SYN: beaded hair, moniliform hair. [L. monile, necklace, + G. thrix, hair] * * * mo·nil·e·thrix mə nil ə .thriks … Medical dictionary
pseudomonilethrix — A nodal trichodystrophy similar to monilethrix but with fractures within the nodal swellings; autosomal dominant inheritance with late onset. * * * pseu·do·mo·nil·e·thrix (soo″do mo nilґə thriks) a condition, inherited as an autosomal… … Medical dictionary
Odonto–Tricho–Ungual–Digital–Palmar syndrome — Classification and external resources OMIM 601957 Odonto–Tricho–Ungual–Digital–Palmar syndrome is an autosomal dominant skin condition with salient clinical features of natal teeth, trichodystrophy, prominent interdigital folds, simian like hands … Wikipedia
