TY  - GEN
ID  - cogprints7015
UR  - http://cogprints.org/7015/
A1  - Dal, SI
A1  - Parmar, P
Y1  - 2010/07/30/
N2  - We have reported a case of Yunis-Varon syndrome which is a rare, autosomal recessive syndrome characterized by growth retardation, defective growth of the cranial bones, characteristic facial features, abnormalities of the fingers and/or toes & cleidocranial dysplasia. Additional features in this case were patent ductus arteriosus, CT brain findings suggestive of ischemic changes, CSF examination suggestive of pyogenic meningitis & cystic changes in right adrenal gland.
PB  - Dr. B.S. Kakkilaya
KW  - Yunis-Varon syndrome
KW  -  distal aphalangea
TI  - Yunis Varon Syndrome
AV  - public
ER  -

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