Neurofibromatosis type 1 and McCune-Albright syndrome occurring in the same patient

British Journal of Dermatology

Volumn 143, Issue 6, 2000, Pages 1288-1291

  Gonzalez Martin, J ^a   Glover, S ^a   Dixon, S ^a   Fryer, A ^a   Carty, H ^a   Smith, C ^a   Kaye, S B ^a   Verbov, J ^a  

^a ALDER HEY CHILDREN S HOSPITAL   (United Kingdom)

Author keywords

McCune Albright syndrome; Neurofibromatosis type 1

Indexed keywords

ALBRIGHT SYNDROME; ARTICLE; CAFE AU LAIT SPOT; CASE REPORT; DISEASE ASSOCIATION; FEMALE; HUMAN; INFANT; NEUROFIBROMATOSIS; NEVUS FLAMMEUS; PRESCHOOL CHILD; PRIORITY JOURNAL;

CHILD; FEMALE; FIBROUS DYSPLASIA, POLYOSTOTIC; HUMANS; MAGNETIC RESONANCE IMAGING; NEUROFIBROMATOSIS 1; OPTIC NERVE GLIOMA; SPHENOID BONE; VISUAL ACUITY;

EID: 0034525401     PISSN: 00070963     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2133.2000.03903.x     Document Type: Article

References (14)

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4. Osteitis fibrosa cystica; the case of a nine year old girl who also exhibits precocious puberty, multiple pigmentation of the skin and hyperthyroidism
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6. The diagnostic value of café-au-lait macules
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11. Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenyl cyclase in McCune-Albright syndrome
12. Diagnosis of von Recklinghausen neurofibromatosis and the Albright syndrome. Two case reports
13. Neurofibromatosis and Albright's syndrome
14. Ocular neurofibromatosis