Marie-unna hereditary hypotrichosis: Case report and review of the literature

Pediatric Dermatology

Volumn 28, Issue 6, 2011, Pages 751-752

  Podjasek, Joshua O ^a   Hand, Jennifer L ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOSTEROID; MINOXIDIL;

ALOPECIA; AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; CORTICOSTEROID THERAPY; DIFFERENTIAL DIAGNOSIS; ELECTRON MICROSCOPY; EYEBROW; EYELASH; GENETIC SCREENING; HAIR LOSS; HUMAN; HYPOTRICHOSIS; LETTER; MARIE UNNA HEREDITARY HYPOTRICHOSIS; PRIORITY JOURNAL; QUALITY OF LIFE; SCALP; SCANTY HAIR;

EID: 81255214471     PISSN: 07368046     EISSN: 15251470     Source Type: Journal    
DOI: 10.1111/j.1525-1470.2011.01602.x     Document Type: Letter

References (2)

1. Redler S, Kruse R, Eigelshoven S, et al., Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 report. J Am Acad Dermatol 2011; 64: e45-e50.
2. Roberts JL, Whiting DA, Henry D, et al., Marie Unna congenital hypotrichosis: clinical description, histopathology, scanning electron microscopy of a previously unreported large pedigree. J Investig Dermatol Symp Proc 1999; 4: 261-267. (Pubitemid 30085817)