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患者:女,19岁,泰旅社员。因出生后双侧唇裂和双手、双足畸形,于78年9月入院。家中几代人均无类似疾患或其它畸形,智力和发育也都正常,父母非近亲联姻,其母妊娠期无何特殊,患者系足月顺产。体检:智力发育正常,左眉弓较为前突,眼裂较小,眼球大小正常,右眼角膜内侧有一点状白斑,双眼视力正常。双侧上唇三度唇裂,上齿槽裂并与鼻腔相通有约2×2厘米的孔。手部:腕部外形活动如常。双侧拇掌骨指化,其末节指向外侧对掌弯屈。
Patient: Female, 19 years old, Thai traveler. Due to bilateral cleft lip and hands after birth, bipedal deformity, was admitted to hospital in September 78. Several generations of family members without any similar diseases or other deformities, intelligence and development are also normal, non-cousins of marriage, their mothers no special pregnancy, patients with full-term delivery. Physical examination: normal mental development, the left eyebrows more prominent protrusion, smaller ocular fissure, normal eye size, right corneal little bit inside the white spot, binocular vision is normal. Bilateral upper lip three cleft lip, upper alveolar cleft and nasal cavity communicating about 2 × 2 cm hole. Hand: wrist shape activities as usual. Bilateral thumb refers to the metacarpal, its distal points to the lateral palmar flexion.