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Case Report
A Case of Hypoglossia-Hypodactylia with t(3q;19p)
Hei-Won Hwang, Ji-Sun Mok, Ji-Eun Kim, Dong-Suk Lee, Doo-Kwun Kim, Sung-Min Choi, Woo-Taek Kim
Clin Exp Pediatr. 2001;44(11):1311-1315.   Published online November 15, 2001
Hypoglossia-hypodactylia syndrome is a congenital disease which is characterized by severe micrognathia, hypoglossia and various anomalies of extremities. This was first reported as 'aglossia congenita' back in 1932 by Rosenthal, and has been reported many times ever since, but has never been reported in Korea. Hall first used the term 'hypoglossia-hypodactylia syndrome', and classified it as one of the oromandibular-limb...
A Case of Pierre Robin Syndrome.
Hyun Hwa Kim, Hae Sook Cha, Byoung Hai Ahn, Young Hee You, Hyun Sook Lee
Clin Exp Pediatr. 1984;27(5):488-492.   Published online May 31, 1984
A case ef Pierre Robin Syndrome in a male baby who was born at the Korea Veterans Hospital was presented. After birth, dyspnea and feeding difficulty were developed. Physical examination revealed micrognathia, glossoptosis and cleft plate. Chromosomal analysis was normal pattern. This finding was compatible with Pierre Robin Syndrome. A brief review of literature was presented.
A case of Pierre-Robin Syndrome.
Soon Ja Han, yeongok bang, Dong Hwan Lee, Sang Jhoo Lee
Clin Exp Pediatr. 1982;25(4):419-422.   Published online April 30, 1982
Micrognathia, cleft palate and glossoptosis, a combination of anomalies known as Pierre Robin syndrome, causes severe respiratory and alimentary difficulties in affected infants. With appropriate care and treatment, mental development can be made normal. But about 10~25% of children become retarded. We have experienced above case in a female infant, aged 6 months. She was acmitted on account of respiratory...
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