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劳·蒙·皮·三氏綜合征,是一个較为少见的病症。在1866年劳蒙二氏首先描写一組綜合症状,他們发现一家三男一女出现相似的症状。主要是夜盲症、視力不足、肥胖、生殖器发育不全、骨骼畸形和智力障碍,且都有視网膜色素变性。1920年Bardet氏分析垂体性肥胖症,认为它是一种先天性原因,在出生后一个月之内就表现出来。这型伴有四肢畸形(多指或併指),并有視网膜色素变性。1920年Biedl氏报告两例生殖无能性肥胖症,并伴有多指,肛門閉鎖,視网膜色素变性、及才智迟鈍。
Laumont-Pitt’s syndrome is a relatively rare condition. In 1866, Lauren II first described a group of syndromes and found that three men and a woman had similar symptoms. Mainly night blindness, poor eyesight, obesity, genital hypoplasia, skeletal deformities and mental retardation, and have retinitis pigmentosa. 1920 Bardet’s analysis of pituitary obesity, that it is a congenital reason, manifested within a month after birth. This type accompanied by limb deformity (multi-finger or finger), and retinitis pigmentosa. In 1920 Biedl reported two cases of reproductive incompetent obesity accompanied by multiple fingers, anal atresia, retinitis pigmentosa, and intellectual retardation.