On mice and men: An autosomal recessive syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anemia [5]

Journal of Pediatrics

Volumn 137, Issue 3, 2000, Pages 441-442

  Majeed, H A ^a   El Shanti, H ^a   Al Rimawi, H ^a   Al Masri, N ^a  

^a UNIVERSITY OF JORDAN   (Jordan)

Author keywords

[No Author keywords available]

Indexed keywords

FERRITIN; HEMOGLOBIN; IRON; LEAD;

DISEASE ASSOCIATION; FERRITIN BLOOD LEVEL; GASTROINTESTINAL ABSORPTION; HUMAN; IRON DEFICIENCY; IRON THERAPY; LEAD BLOOD LEVEL; LEAD POISONING; LETTER; PRIORITY JOURNAL;

EID: 0033831130     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1067/mpd.2000.107613     Document Type: Letter

References (7)

1. Congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis in three related children and the association with Sweet syndrome in two siblings
2. Dyserythropoeisis and dyserythropoietic anaemia
3. HEMPAS congenital dyserythropoietic anaemia (type II)
4. Chronic recurrent multifocal osteomyelitis associated with tumoral calcinosis
5. Multifocal chronic periostitis responsive to colchicine
6. Recurrent multifocal periostosis in children. Report of a familial form
7. Chronic multifocal osteomyelitis, a new recessive mutation on chromosome 18 of the mouse