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Hereditary pubertal genu valgum in Iran
Author(s) -
Ghorbani K.,
Carapetian J.
Publication year - 1994
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.1399-0004.1994.tb04021.x
Subject(s) - genu valgum , offspring , dysplasia , medicine , deformity , ankle , anatomy , biology , genetics , orthodontics , surgery , pregnancy
Two male offspring of a healthy father in Galaz, a remote village in Northwest Iran, were noted to show severe asymmetric genu valgum, with 57 and 82 degrees angulation and dysplasia of the lateral femoral condyle, together with adaptive biomechanical changes of the ankle alignment. Three of the five male offspring of a second marriage who have reached puberty also show variable degrees of genu valgum, increasing with growth. The intermalleolar distance in the affected sons aged 16, 15, and 12 measured 21, 16, and 14 cm, respectively, before epiphysodesis. None of the six female offspring from either marriage, and neither of the two sons under the age of 11 from the second marriage show any skeletal deformity. All members of the family are otherwise mentally and physically normal. It is possible that this genu valgum may be due to a new autosomal dominant mutation which probably occurred in the gonads of the unaffected father. The condition shows an onset age of 11 and appears to have a sex‐limited expression.