Objective: Our aim was to investigate the microscopic surface structural alteration in hair with hereditary trichodysplasia. This article presents the results of light and scanning electron microscopy (SEM) examination of cases having hereditary trichodysplasia. Methods: The biopsy specimens were obtained from 2 girls of ages 3 and 5-years, Department of Pediatrics, Faculty of Medicine, Hacettepe University in 2001. A large number of hair specimens were obtained from these 2 cases having hereditary trichodysplasia. Routine light microscopic and SEM procedure was performed on the tissue specimen, and then they were examined by light microscopy and SEM. Results: Hair specimens taken from both patients had great similarities. Our results revea...
Abstract: We report a family affected to the fourth generation by uncombable hair syndrome. This sy...
Trichothiodystrophy (TTD) is a rare multisystem disorder with an autosomal recessive mode of inherit...
Marie Unna congenital hypotrichosis (MUCH) is a rare autosomal dominant condition in which abnormali...
Objective: Our aim was to investigate the microscopic structural alteration in hair with hereditary ...
This is a study of eight members of one family with Marie Unna hypotrichosis occurring in five gener...
In many disorders with a genetic background the sparsity of scalp hairs may deter the clinician from...
A 24-year-old boy applied for his nevuses. On dermatological examination, he was noticed to have gli...
Pili annulati, monilethrix and trichothiodystrophy are uncommon conditions in which the hair shaft h...
Background: Trichothiodistrophy (TTD) is a rare autosomal recessive condition that is characterized ...
Trichothiodystrophy, also called sulphur-deficient brittle hair syndrome, is a rare autosomal recess...
We examined hair from 15 patients with trichothiodystrophy (TTD), a rare inherited disorder with bri...
Analysis of single hair fibres in genetic disorders is a desirable complement to the clinical diagno...
Hair from a four year old white girl with a history of brittle hair since birth did not show any pre...
BACKGROUND: Pili annulati is an inherited hair shaft abnormality with a wide range of clinical expre...
We have used the scanning electron microscope to investigate the changes that occur in scalp hair du...
Abstract: We report a family affected to the fourth generation by uncombable hair syndrome. This sy...
Trichothiodystrophy (TTD) is a rare multisystem disorder with an autosomal recessive mode of inherit...
Marie Unna congenital hypotrichosis (MUCH) is a rare autosomal dominant condition in which abnormali...
Objective: Our aim was to investigate the microscopic structural alteration in hair with hereditary ...
This is a study of eight members of one family with Marie Unna hypotrichosis occurring in five gener...
In many disorders with a genetic background the sparsity of scalp hairs may deter the clinician from...
A 24-year-old boy applied for his nevuses. On dermatological examination, he was noticed to have gli...
Pili annulati, monilethrix and trichothiodystrophy are uncommon conditions in which the hair shaft h...
Background: Trichothiodistrophy (TTD) is a rare autosomal recessive condition that is characterized ...
Trichothiodystrophy, also called sulphur-deficient brittle hair syndrome, is a rare autosomal recess...
We examined hair from 15 patients with trichothiodystrophy (TTD), a rare inherited disorder with bri...
Analysis of single hair fibres in genetic disorders is a desirable complement to the clinical diagno...
Hair from a four year old white girl with a history of brittle hair since birth did not show any pre...
BACKGROUND: Pili annulati is an inherited hair shaft abnormality with a wide range of clinical expre...
We have used the scanning electron microscope to investigate the changes that occur in scalp hair du...
Abstract: We report a family affected to the fourth generation by uncombable hair syndrome. This sy...
Trichothiodystrophy (TTD) is a rare multisystem disorder with an autosomal recessive mode of inherit...
Marie Unna congenital hypotrichosis (MUCH) is a rare autosomal dominant condition in which abnormali...