Puvabanditsin Surasak, Gorbonosov Michelle, Blackledge Kristin, Manzano Jeffrey, Federici Matthew, Mehta Rajeev
Department of Pediatrics Rutgers RWJ Medical School New Brunswick New Jersey USA.
Department of Family Medicine Rutgers RWJ Medical School New Brunswick New Jersey USA.
Clin Case Rep. 2022 Jul 11;10(7):e6000. doi: 10.1002/ccr3.6000. eCollection 2022 Jul.
We report a preterm male neonate presenting with a short trunk, short neck, low hairline, deformed ears, preauricular skin tag, penoscrotal transposition (PT), palmar crease, short and broad fingers and toes (brachydactyly), hypoplastic and deep-set nails, metatarsal abductus, and cross-fused, small echogenic kidneys. Radiologic findings and genetic studies are consistent with spondylocostal dysostosis (SCD) and autosomal dominant brachydactyly. This is the first case report of spondylocostal dysostosis and brachydactyly associated with and variants. We reviewed the literature and compared our patient's phenotype with previously reported cases of SCD.
我们报告了一名早产男婴,其表现为躯干短、颈部短、发际线低、耳朵畸形、耳前皮肤赘生物、阴茎阴囊转位(PT)、掌纹、手指和脚趾短而宽(短指畸形)、指甲发育不全且深陷、跖骨外展以及交叉融合的小回声肾。放射学检查结果和基因研究与脊椎肋骨发育不良(SCD)和常染色体显性短指畸形相符。这是首例关于脊椎肋骨发育不良和短指畸形与[此处原文可能缺失相关基因名称]变体相关的病例报告。我们回顾了文献,并将我们患者的表型与先前报道的SCD病例进行了比较。