Loose anagen syndrome (LAS) is a hair disorder involving insufficient anchoring of the hair follicle to the scalp owing to an autosomal dominant or sporadic mutation in the gene encoding keratin 6. There are three phenotypes of LAS, including type B, which presents in young, light-haired girls as unruly, uncombable hair with diminished growth. We present a 2-year-old girl with LAS type B whose identical twin sister was unaffected. The diagnosis was confirmed with a painless hair pull test proven to contain anagen hairs with ruffled cuticles on trichoscopy, preventing the need for unnecessary referrals and diagnostic tests
Griscelli Syndrome (GS) is a rare autosomal recessive disorder characterized by pigmentary dilution ...
Summary. A 7-year-old girl was admitted to the hospital for anaemia, secon-dary to intestinal blood ...
Moyamoya disease is a unique chronic cerebrovascular condition caused by progressive stenosis of the...
BACKGROUND/OBJECTIVES: Loose anagen syndrome (LAS) is a disorder of abnormal anchorage of the hair t...
Loose anagen hair syndrome (LAHS) is characterized by easily extractable anagen hairs that lose the ...
To help determine the specificity of “loose anagen” (LA) hairs in Loose Anagen Syndrome, the presenc...
Loose anagen hair syndrome (LAHS) is an underestimated cause of noncicatricial alopecia among childr...
To the Editor: We describe two patients with epidermolysis bullosa simplex, Dowling-Meara type (EBS-...
Congenital abnormalities of the hair shaft are conditions in most cases linked to chemical, biochemi...
none7noBackground: The short anagen syndrome (SAS) is a rare idiopathic pediatric disorder characte...
Griscelli syndrome (GS) is a rare autosomal recessive disorder caused by mutation in the MYO5A (GS1,...
Short anagen syndrome is a relatively recently described entity. This syndrome is an unusual conditi...
The differential diagnosis of a strongly positive and painless hair pull test includes alopecia area...
Androgenetic alopecia (AGA) is the most common type of hair loss in adults. Although there are diffe...
Keratitis ichthyosis deafness syndrome is a rare congenital ectodermal disorder. It appears to be ge...
Griscelli Syndrome (GS) is a rare autosomal recessive disorder characterized by pigmentary dilution ...
Summary. A 7-year-old girl was admitted to the hospital for anaemia, secon-dary to intestinal blood ...
Moyamoya disease is a unique chronic cerebrovascular condition caused by progressive stenosis of the...
BACKGROUND/OBJECTIVES: Loose anagen syndrome (LAS) is a disorder of abnormal anchorage of the hair t...
Loose anagen hair syndrome (LAHS) is characterized by easily extractable anagen hairs that lose the ...
To help determine the specificity of “loose anagen” (LA) hairs in Loose Anagen Syndrome, the presenc...
Loose anagen hair syndrome (LAHS) is an underestimated cause of noncicatricial alopecia among childr...
To the Editor: We describe two patients with epidermolysis bullosa simplex, Dowling-Meara type (EBS-...
Congenital abnormalities of the hair shaft are conditions in most cases linked to chemical, biochemi...
none7noBackground: The short anagen syndrome (SAS) is a rare idiopathic pediatric disorder characte...
Griscelli syndrome (GS) is a rare autosomal recessive disorder caused by mutation in the MYO5A (GS1,...
Short anagen syndrome is a relatively recently described entity. This syndrome is an unusual conditi...
The differential diagnosis of a strongly positive and painless hair pull test includes alopecia area...
Androgenetic alopecia (AGA) is the most common type of hair loss in adults. Although there are diffe...
Keratitis ichthyosis deafness syndrome is a rare congenital ectodermal disorder. It appears to be ge...
Griscelli Syndrome (GS) is a rare autosomal recessive disorder characterized by pigmentary dilution ...
Summary. A 7-year-old girl was admitted to the hospital for anaemia, secon-dary to intestinal blood ...
Moyamoya disease is a unique chronic cerebrovascular condition caused by progressive stenosis of the...