Takahashi Masahiro, Ariwa Masataka, Yamaguchi Tetsutaro
Department of Orthodontics, School of Dentistry, Kanagawa Dental University, Yokosuka, JPN.
Cureus. 2024 Feb 2;16(2):e53467. doi: 10.7759/cureus.53467. eCollection 2024 Feb.
Shwachman-Diamond syndrome (SDS) is a rare autosomal recessive disorder mainly caused by mutations in the Shwachman-Bodian-Diamond syndrome gene on chromosome 7q11. Although skeletal abnormalities are a feature of SDS, no reports have focused on the craniofacial morphology of patients with SDS. Moreover, the detailed dental characteristics of SDS remain unknown. In the present case report, we evaluated the craniofacial morphology and dental findings of two patients with SDS. A Japanese adolescent sibling pair with SDS had the chief complaint of excessive overjet. Cephalometric analysis revealed similar craniofacial morphology in both patients: skeletal class I malocclusion with a hypodivergent pattern and labial inclination of the maxillary and mandibular incisors. A panoramic photograph showed the tendency of delayed permanent tooth eruption and replacement in both patients. These cases suggest that malocclusion requiring orthodontic treatment might be a feature of patients with SDS.
施瓦赫曼-戴蒙德综合征(SDS)是一种罕见的常染色体隐性疾病,主要由7号染色体长臂11区的施瓦赫曼-博迪安-戴蒙德综合征基因突变引起。虽然骨骼异常是SDS的一个特征,但尚无报告聚焦于SDS患者的颅面形态。此外,SDS详细的牙齿特征仍不清楚。在本病例报告中,我们评估了两名SDS患者的颅面形态和牙齿表现。一对患有SDS的日本青少年同胞姐妹主要主诉为前牙深覆盖过度。头影测量分析显示两名患者的颅面形态相似:骨骼I类错牙合,呈低角型,上颌和下颌切牙唇倾。全景片显示两名患者均有恒牙萌出和替换延迟的倾向。这些病例表明,需要正畸治疗的错牙合可能是SDS患者的一个特征。