Al-Qattan Mohammad M, Maddirevula Sateesh, Alkuraya Fowzan S
Division of Plastic Surgery at King Saud University, Riyadh, Saudi Arabia; Division of Plastic Surgery at King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Eur J Med Genet. 2020 Jan;63(1):103615. doi: 10.1016/j.ejmg.2019.01.005. Epub 2019 Jan 14.
Ulnar-mammary syndrome (UMS) is a rare syndromic limb malformation caused by heterozygous mutations in TBX3. The name highlights the two commonly involved body parts i.e. mammary gland and ulnar ray of the upper limbs, although a more extensive systemic involvement is also known to occur. Here, we report the surprising finding of a patient with a de novo mutation in TBX3 whose clinical presentation is limited to dorsalization of both little fingers and slightly deep 4th web spaces. We review the literature to confirm that this should be considered as a forme fruste phenotype of UMS.
尺骨-乳腺综合征(UMS)是一种由TBX3基因杂合突变引起的罕见综合征性肢体畸形。该名称突出了两个常见受累的身体部位,即乳腺和上肢的尺骨射线,尽管也已知会出现更广泛的全身受累情况。在此,我们报告了一名TBX3基因新发突变患者的惊人发现,其临床表现仅限于双侧小指背屈和第4指蹼间隙略深。我们回顾文献以确认这应被视为UMS的顿挫型表型。