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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2010
2010
Eyelashes hypotrichosis is a condition indicated by an inadequate amount of eyelashes. Hypertrichosis of eyelashes, characterized… (More)
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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… (More)
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2009
2009
Congenital ichthyosis encompasses a heterogeneous group of disorders of cornification. Isolated forms and syndromic ichthyosis… (More)
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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… (More)
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2007
2007
Human autosomal recessive ichthyosis with hypotrichosis (ARIH) is an inherited disorder recently linked to homozygosity for a… (More)
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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… (More)
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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… (More)
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2002
2002
Hypotrichosis with juvenile macular dystrophy is a rare autosomal recessive disorder characterized by early hair loss heralding… (More)
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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… (More)
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1999
1999
Hereditary congenital hypotrichosis is an autosomal dominant pilar dysplasia first described by Marie Unna in an extended German… (More)
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