TY  - GEN
AU  - Sismanis,A
AU  - Polisar,I A
AU  - Ruffy,M L
AU  - Lambert,J C
TI  - Rare congenital syndrome associated with profound hearing loss
SN  - 0003-9977
PY  - 1979///0523
KW  - Abnormalities, Multiple
KW  - Child, Preschool
KW  - Deafness
KW  - etiology
KW  - Humans
KW  - Lipase
KW  - deficiency
KW  - Lipid Metabolism, Inborn Errors
KW  - complications
KW  - Malabsorption Syndromes
KW  - Male
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1001/archotol.1979.00790160056015
ER  -