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The Nathalie syndrome. A new hereditary syndrome
Author(s) -
Cremers C. W. R. J.,
Haar B. G. A. ter,
Rens T. J. G. van
Publication year - 1975
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1975.tb01511.x
Subject(s) - medicine , genetics , pediatrics , biology
Deafness, cataract, muscular atrophy, skeletal abnormalities, retardation of growth, underdeveloped secondary sexual characteristics, and electrocardiographic abnormalities are the features of a new, probably hereditary syndrome. Case reports are presented.