Incontinentia pigmenti. A rare disease with many symptoms;Incontinentia pigmenti. En ovanlig sjukdom med många symtom.

Läkartidningen

Volumn 99, Issue 12, 2002, Pages 1345-1350

  Holmström, Gerd ^a   Bergendal, Birgitta ^a   Hallberg, Gunilla ^a   Marcus, Suzanne ^a   Hallén, Anders ^a   Dahl, Niklas ^a  

^a UPPSALA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN DISEASE; CHILD; DENTITION; DIFFERENTIAL DIAGNOSIS; EYE DISEASE; FEMALE; GENE DELETION; GENETICS; HUMAN; INCONTINENTIA PIGMENTI; INFANT; MALE; NEWBORN; NUCLEOTIDE SEQUENCE; PATHOLOGY; PRACTICE GUIDELINE; PRESCHOOL CHILD; REVIEW; SKIN; TOOTH DISEASE; VISUAL DISORDER;

BRAIN DISEASES; CHILD; CHILD, PRESCHOOL; DENTITION; DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; EYE DISEASES; FEMALE; GENE DELETION; HUMANS; INCONTINENTIA PIGMENTI; INFANT; INFANT, NEWBORN; MALE; PRACTICE GUIDELINES; SKIN; TOOTH DISEASES; VISION DISORDERS;

EID: 0037149653     PISSN: 00237205     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (13)