Trichothiodystrophy (TTD) is a rare multisystem disorder with an autosomal recessive mode of inheritance. TTD presentations vary from only hair abnormalities like brittle, fragile hair to physical and mental retardation. Mutations of DNA repair genes have been identified as responsible for the disease. A 5-year-old boy presented with sparse, short, and brittle hair to our clinic. He was born to consanguineous parents. Trichoscopy and light microscopy revealed broken hairs with no specific shaft defect. Due to the inaccessibility of the polarized microscopy, a bedside technique was employed. We used a polarized dermatoscope and a mirror in order of achieving transillumination of the hair shafts, which revealed striking bright and dark bands....
Background: Trichothiodistrophy (TTD) is a rare autosomal recessive condition that is characterized ...
Trichothiodystrophy (TTD) is a rare autosomal recessive disorder characterized by brittle hair, ment...
Objective: Our aim was to investigate the microscopic structural alteration in hair with hereditary ...
We describe a case of trichothiodystrophy occuring as an isolated disorder. A 19-year old man has ha...
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...
Abstract: Trichothiodystrophy refers to a heterogeneous group of rare genetic diseases that affects ...
Abstract. Trichothiodystrophy (TTD) is a rare, autosomal recessive, multisystem disorder characteriz...
Definition and diagnosis The term trichothiodystrophy (TTD) was coined by Price in 1979-19801-3 base...
These authors contributed equally to this work. Trichothiodystrophy (TTD) is a rare multisystem diso...
Trichothiodystrophy (TTD) is a rare, autosomal recessive, multisystem disorder characterized by sulf...
Trichothiodystrophy (TTD) is a group of rare autosomal recessive disorders that variably affect a wi...
Trichothiodystrophy (TTD) is a rare autosomal recessive disease characterized by brittle hair with r...
Trichothiodystrophy (TTD) is a rare autosomal recessive disorder whose defining feature is brittle h...
Trichothiodystrophy (TTD), an autosomal recessive disorder characterized by sulfur-deficient brittle...
Background: Trichothiodistrophy (TTD) is a rare autosomal recessive condition that is characterized ...
Trichothiodystrophy (TTD) is a rare autosomal recessive disorder characterized by brittle hair, ment...
Objective: Our aim was to investigate the microscopic structural alteration in hair with hereditary ...
We describe a case of trichothiodystrophy occuring as an isolated disorder. A 19-year old man has ha...
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...
Abstract: Trichothiodystrophy refers to a heterogeneous group of rare genetic diseases that affects ...
Abstract. Trichothiodystrophy (TTD) is a rare, autosomal recessive, multisystem disorder characteriz...
Definition and diagnosis The term trichothiodystrophy (TTD) was coined by Price in 1979-19801-3 base...
These authors contributed equally to this work. Trichothiodystrophy (TTD) is a rare multisystem diso...
Trichothiodystrophy (TTD) is a rare, autosomal recessive, multisystem disorder characterized by sulf...
Trichothiodystrophy (TTD) is a group of rare autosomal recessive disorders that variably affect a wi...
Trichothiodystrophy (TTD) is a rare autosomal recessive disease characterized by brittle hair with r...
Trichothiodystrophy (TTD) is a rare autosomal recessive disorder whose defining feature is brittle h...
Trichothiodystrophy (TTD), an autosomal recessive disorder characterized by sulfur-deficient brittle...
Background: Trichothiodistrophy (TTD) is a rare autosomal recessive condition that is characterized ...
Trichothiodystrophy (TTD) is a rare autosomal recessive disorder characterized by brittle hair, ment...
Objective: Our aim was to investigate the microscopic structural alteration in hair with hereditary ...