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Case Report
A Case of Potter Syndrome Associated with Renal Dysplasia.
Young Woo Park, Joon Ho Kim, Eun Ryoung Kim, Soon Jae Lee, Young Chul Moon, Young Jin Kim
Clin Exp Pediatr. 1987;30(7):812-817.   Published online July 31, 1987
Potter syndrome is relatively rare congenital defect in with agenesis or dysplasia of the kidney is associated with oligohydramnios, pulmonary hypoplasia, characteristic facial features and other abnormalities. The etiology is unknown. But various theories are reviewed and the suggestion is made that the cause of Potter syndrome in newborns may well be multifactorial. Among the various factors, we agree to the opinion that oligohydramnios...
A Case of Potter Syndrome Type I.
Jong Cheol Ryu, Jae Kwang Hong, Jun Taek Park, Jung Sik Min, Chang Jee Choi, Je Geun Chi
Clin Exp Pediatr. 1986;29(10):1152-1156.   Published online October 31, 1986
We have experienced a case of Potter syndrome type I in a newborn infant who presented with severe respiratory distress soon after birth. The diagnosis was made with autopsy findings consisted of bilateral polycystic renal dysplasia, bilateral hypoplastic lung , facies renalis, fibrocystic change of liver, patent ductus arteriosus, patent foramen ovale, ureter and urinary bladder hypoplasia and calcaneovarus. Brief...
Original Article
Renovascular Hypertension in Childhood.
Jae Won Song, Soo Heun Lim, Yong Choi, Kwang Wook Ko, Chang Yee Hong, Kyung Mo Yeon
Clin Exp Pediatr. 1986;29(4):381-386.   Published online April 30, 1986
The following results were obtained from a retrospective analysis of 21 cases of renovascular hypertension who were admitted to Pediatric Department, Seoul National University Hospital, during the period from January 1978 to December 1985. 1) Takayasu arteritis was the most common cause (15 out of 21, 71%), and fibromuscular dysplasia of renal artery was confirmed only in two (9.5%) cases. 2) Male...
Case Report
A Case of Spondylothoracic Dysplasia.
Jong Sic Joo, Bong Joon Chung, Yong Sub Kim, Kyung Hye Park, Chan Yung Kim
Clin Exp Pediatr. 1985;28(12):1221-1224.   Published online December 31, 1985
The author experienced a case of spondylothoracic dysplasia from 4 month old female-patient who had congenital anomalies on vertebrae & thorax. She was born with normal weight and full term, but she looked bizarre because of shortened trunk & neck, marked protuberant abdomen, prominent lumbar lordosis. On admission, she had growth retardation for having upper respiratory tract infection and feeding...
A Case of Genetic Skeletal Dysplasias.
Jeh Hoon Sin
Clin Exp Pediatr. 1985;28(11):1125-1129.   Published online November 30, 1985
Genetic skeletal dysplasias(osteochondrodysplasias) are a heterogenous group of conditions characterized by disordered growth of the various components of the skeleton, leading to disproportionate short status, deformity, or other structural and functional abnormalities of individual skeletal elements. Author experienced a case of the genetic skeletal dysplasia newborn who was born in Dong Bu City Hospital.
Two Case of Watson-Alagille Syndrome.
Heon Seok Han, Soo Heum Lim, Young Sun Kim, Jeong Kee Seo, Hyung Ro Moon
Clin Exp Pediatr. 1985;28(10):1047-1051.   Published online October 31, 1985
Watson-Alagille syndrome (Arteriohepatic dysplasia, Syndromatic paucity of interlobular bile duct), a disease characterized by chronic liver disease, characteristic facies, cardiova scular abnormalities, and vertebral arch abnormalities has paucity of interlobular bile ducts on histologic examination of liver. We experienced two cases of Watson-Alagille syndrome in a 7-month-old male infant and a 12-month-old male infant who had the chief complaint of...
A Case of Thanatophoric Dysplasia.
Hae Sook Cha, Hyun Hwa Kim, Young Hee You, Hyun Sook Lee, Jeong Rae Kim
Clin Exp Pediatr. 1984;27(5):521-526.   Published online May 31, 1984
A case of thanatophoric dysplasia was presented with a brief review of literature. The baby showed characteristic clinical feature with relatively large head, prominent forehead, flattening of the bridge of the nose and extremly short arm and legs. X-ray showed marked shortening of rib, narrow chest, flattened vertebral body within lumbar region, rectangular shape of pelvic bone, prominent softtissue of abdomen...
Acromesomelic Dysplasia Syndrome.
Hyung Ro Moon
Clin Exp Pediatr. 1984;27(1):98-104.   Published online January 31, 1984
A further case of acromesomelic dysplasia syndrome is reported in a twelve year old Korean boy born on January 15, 1971 at full term. His height was only 99.5 cm. on his visit to the outpatient department. The present case showed disproportionate shortening of the extremities, especially in the forearms, hands, shanks and feet together with most of the reported...
A Cases of Heredotary Anhidrotic Ectodermal Dyslasia.
Jong Soo Kim, Pyoung Han Hwang, Hyeon Sook Lee, Jung Soo Kim
Clin Exp Pediatr. 1983;26(10):1018-1023.   Published online October 31, 1983
Hereditary anhidrotic ectodermal dysplasia is a rare hereditary condition in which certain structures derived from the ectoderm are undeveloped or underdeveloped, although, on a rarity, mesodermal or endodermal derivatives may be associated. Recently, we have experienced a case of anhidrotic ectodermal dysplasia in 4 years old male. He had abscence of sweating, hypotrichosis and anodontia, which was characteristic features of this disorder. We established...
There cases of Hereditary Anhidrotic Ectodermal Dysplasia.
Seung Woo Moon, Seung Koo Park, Jung Ju Kim, Dong Hak Shin, Sang Suk Lee
Clin Exp Pediatr. 1982;25(1):80-88.   Published online January 31, 1982
Hereditary anhidrotic ectodermal dysplasia is a rare hereditary condition in which certain structures derived from the ectoderm are undeveloped or underdeveloped, although, on a rarity, mesodermal or endodermal derivatives may be associated. Recently, we enperienced 3-cases of anhidrotic ectodermal dysplasia in 3 months male infant and in brothers aged 4(1/2) months and 22 months. They had abscence of sweating, hypotrichosis...