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Hypotrichosis

Known as: Hypotrichosis, infantile, Congenital hypotrichosis, Scanty hair 
A congenital condition, usually due to genetic aberrations, that is characterized by a lack of hair growth on the head and/or body.
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Post-transcriptional processing of some long non-coding RNAs (lncRNAs) reveals that they are a source of miRNAs. We show that the… Expand
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Highly Cited
2009
Highly Cited
2009
Marie Unna hereditary hypotrichosis (MUHH) is an autosomal dominant form of genetic hair loss. In a large Chinese family carrying… Expand
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Highly Cited
2009
Highly Cited
2009
Woolly hair (WH) is characterized by the presence of fine and tightly curled hair. WH can appear as a symptom of some systemic… Expand
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Highly Cited
2009
Highly Cited
2009
Congenital ichthyosis encompasses a heterogeneous group of disorders of cornification. Isolated forms and syndromic ichthyosis… Expand
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Highly Cited
2008
Highly Cited
2008
BACKGROUND NB-UVB phototherapy is a very important modality in treating vitiligo but the treatment course usually exceeds 1 year… Expand
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Highly Cited
2007
Highly Cited
2007
In this article, we describe a novel autosomal recessive ichthyosis with hypotrichosis syndrome, characterized by congenital… Expand
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Highly Cited
2007
Highly Cited
2007
Human autosomal recessive ichthyosis with hypotrichosis (ARIH) is an inherited disorder recently linked to homozygosity for a… Expand
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Highly Cited
2003
Highly Cited
2003
Cell adhesion and communication are interdependent aspects of cell behavior that are critical for morphogenesis and tissue… Expand
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Highly Cited
2003
Highly Cited
2003
We have identified nonsense mutations in the gene CDSN (encoding corneodesmosin) in three families suffering from hypotrichosis… Expand
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Highly Cited
2001
Highly Cited
2001
Congenital hypotrichosis associated with juvenile macular dystrophy (HJMD; MIM601553) is an autosomal recessive disorder of… Expand
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