Bilateral Cryptorchidism in Silver-Russell Syndrome: Initial Experience with Laparoscopic Orchiopexy
ÀÌÁß±Ù, ÀÌ»óÇù, Àü½ÂÇö, ±èÁøÀÏ, À¯±¸ÇÑ,
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ÀÌÁß±Ù ( Lee Joong-Geun )
°æÈñ´ëÇб³ ÀÇ°ú´ëÇÐ ºñ´¢±â°úÇб³½Ç
ÀÌ»óÇù ( Lee Sang-Hyub )
°æÈñ´ëÇб³ ÀÇ°ú´ëÇÐ ºñ´¢±â°úÇб³½Ç
Àü½ÂÇö ( Jeon Seung-Hyun )
°æÈñ´ëÇб³ ÀÇ°ú´ëÇÐ ºñ´¢±â°úÇб³½Ç
±èÁøÀÏ ( Kim Jin-Il )
°æÈñ´ëÇб³ ÀÇ°ú´ëÇÐ ºñ´¢±â°úÇб³½Ç
À¯±¸ÇÑ ( Yoo Koo-Han )
°æÈñ´ëÇб³ ÀÇ°ú´ëÇÐ ºñ´¢±â°úÇб³½Ç
KMID : 0358320090500060615
Abstract
Silver-Russel syndrome (SRS) is a disorder present at birth that involves poor growth, low birth weight, differences in the size of the two sides of the body, and genital anomalies. The diagnosis is based on distinct prenatal growth restriction and the presence of typical dysmorphic features, including short stature and limb asymmetry. We report a case of bilateral cryptorchidism with no other genital anomalies in SRS. This report provides an overview of the genital anomalies of SRS and describes, for the first time, a laparoscopic orchiopexy in SRS.
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Cryptorchidism;Dwarfism;Fetal growth retardation;Laparoscopy
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