Cohen syndrome and rheumatoid arthritis [2]

Genetic Counseling

Volumn 13, Issue 1, 2002, Pages 63-64

  De Ravel, T J L ^a   Azou, M ^a   Fryns, J P ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHILD; CLINICAL FEATURE; COHEN SYNDROME; CRANIOFACIAL MALFORMATION; DISEASE ASSOCIATION; EYE DISEASE; HUMAN; JUVENILE RHEUMATOID ARTHRITIS; LETTER; MALE;

ABNORMALITIES, MULTIPLE; ARTHRITIS, JUVENILE RHEUMATOID; FACIES; HUMANS; INFANT, NEWBORN; MALE; MICROCEPHALY; SYNDROME;

EID: 0036206083     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (6)

1. Confirmation of the Cohen syndrome
2. A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb abnormalities
3. Juvenile arthritis - Who gets it, where and when? A review of current data on incidence and prevalence
4. Cohen syndrome: Essential features, natural history, and heterogeneity
5. Cohen syndrome: Further delineation and inheritance
6. Comparative epidemiology of the rheumatic diseases in children