Unusual Association of Orofacial Cleft and Finger-Like Skin Appendages With or Without Constriction Rings: A Disorganization-Like Phenotype?

IF 1.3 4区 医学 Q2 Dentistry
Cleft Palate-Craniofacial Journal Pub Date : 2026-11-01 Epub Date: 2026-03-29 DOI:10.1177/10556656261437279
Henrique Regonaschi Serigatto, Siulan Vendramini-Pittoli, Priscila Padilha Moura, Luiza Virmond, Vinicius Contrucci Dantas Segarra, José Humberto da Cunha, Carla Rosenberg, Roseli Maria Zechi-Ceide, Nancy Mizue Kokitsu-Nakata
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引用次数: 0

Abstract

The mouse disorganization (Ds) was described in mutant mice with multiple congenital anomalies arising from the 3 germinative layers. The human homologue of Ds was proposed in a case presenting multiple congenital anomalies associated with the unique feature of a finger-like skin appendage. Since then, several cases have been reported suggesting the occurrence of a disorganization-like (Ds-like) phenotype in humans. Here, we report a case series of 7 patients presenting with the association of orofacial clefts and finger-like skin appendages. These cases, despite the similarities with Ds and amniotic band sequence, may represent a distinct condition within the spectrum of Ds-like, as other cases previously reported in the literature.

有或没有收缩环的口面裂和指状皮肤附属物的不寻常关联:一种无序样表型?
小鼠组织紊乱(Ds)在突变小鼠中被描述为由3个萌发层引起的多种先天性异常。在一个病例中提出了Ds的人类同源物,该病例呈现出与手指样皮肤附属物的独特特征相关的多种先天性异常。从那时起,有几例报告表明在人类中出现了一种无组织样(ds样)表型。在这里,我们报告了一个病例系列,7例患者提出的联合口面裂和指状皮肤附属物。尽管这些病例与Ds和羊膜带序列相似,但与文献中先前报道的其他病例一样,这些病例可能在Ds样谱系中代表一种独特的病症。
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来源期刊
Cleft Palate-Craniofacial Journal
Cleft Palate-Craniofacial Journal DENTISTRY, ORAL SURGERY & MEDICINE-SURGERY
CiteScore
2.20
自引率
36.40%
发文量
0
审稿时长
4-8 weeks
期刊介绍: The Cleft Palate-Craniofacial Journal (CPCJ) is the premiere peer-reviewed, interdisciplinary, international journal dedicated to current research on etiology, prevention, diagnosis, and treatment in all areas pertaining to craniofacial anomalies. CPCJ reports on basic science and clinical research aimed at better elucidating the pathogenesis, pathology, and optimal methods of treatment of cleft and craniofacial anomalies. The journal strives to foster communication and cooperation among professionals from all specialties.
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