. 2002; 17(3): 189-191 | |||
Laurence Moon Biedl SyndromeEsra Önal Sönmez1, Nihal Karatoprak2, Sami Hatipoğlu1, H. Mine Öztürk1, Ela Erdem1, Günsel Kutluk1, Tülay Olgun1, Ahmet Özgüner21Sisli Etfal Education and Research Hospital4. Children's Clinic, Istanbul2Haydarpasa Numune Training and Research Hospital, 1.Children's Clinic, Istanbul Laurence Moon Biedl syndrome, an autosomal recessive disorder, characterized by retinitis pigmentosa, obesity, polidactyly, hypogonadism and mental retardation. A 5.5 years old male child was admitted to hospital because of pneumonia. During his hospitalization, symtoms of night blindness were detected. Retinitis pigmentosa was determined in his visual examination. He had been operated because of polidactyly Laurence Moon Biedl SendromuEsra Önal Sönmez1, Nihal Karatoprak2, Sami Hatipoğlu1, H. Mine Öztürk1, Ela Erdem1, Günsel Kutluk1, Tülay Olgun1, Ahmet Özgüner21Şişli Etfal Eğitim ve Araştırma Hastanesi 4. Çocuk Kliniği, İstanbul2Haydarpaşa Numune Eğitim ve Araştırma Hastanesi 1. Çocuk Kliniği, İstanbul Anahtar Kelimeler: Laurence Moon Biedl Sendromu, obezite, polidaktili, retinitis pigmentosa Esra Önal Sönmez, Nihal Karatoprak, Sami Hatipoğlu, H. Mine Öztürk, Ela Erdem, Günsel Kutluk, Tülay Olgun, Ahmet Özgüner. Laurence Moon Biedl Syndrome. . 2002; 17(3): 189-191 Corresponding Author: Esra Önal Sönmez, Türkiye |
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