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1 "Kallmanns syndrome"
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Original Article
Kallmann's Syndrome Associasted with Slipped Capital Femoral Epiphysis.
Hyeon Jeong Jeon, Byeong Seong Ko, Do Hyeong Kim, Jang Hwan Bae, TGae Geun Oh, Seung Baek Kang
J Korean Endocr Soc. 1996;11(3):318-323.   Published online November 7, 2019
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The Kallmanns syndrome is the most common form of isolated hypogonadotropic hypogonadism in which anosmia or hyposmia resulting from agenesis of hypoplasia of the olfactory lobes is associated with LHRH deficiency, This syndrome is genetically heterogeneous and can be trans-mitted as an X-linked, autosomal dominant or autosomal recessive trait. The hypogonadotropic hypogonadism results in absent or incomplete pubertal development and may be associated with anosmia or hyposmia, mid-line defect(color blindness, cleft-lip or -palate, unilateral renal agenesis, nerve deafness), cryptorchidism and skeletal abnormalities. The slipped capital fernoral epiphysis is the condition in which the femoral head slips downward and backward on the femoral neck at the epiphyseal plate. The clinical association between slipped capital femoral epiphysis and endocrine disorder. We experienced a case of the slipped capital femoral epiphyis associated with Kallmanns syndrome in a 17 years old male.
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