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Quoted phrase not found in phrase index: "1-3 toe syndactyly"
Page 1
Clinical Manifestations of Constriction Band Syndrome.
Demetri LRF, Starcevich AG, Manske MCB, James MA. Demetri LRF, et al. J Bone Joint Surg Am. 2022 Jul 20;104(14):1301-1310. doi: 10.2106/JBJS.21.01286. Epub 2022 Apr 14. J Bone Joint Surg Am. 2022. PMID: 35856931
There was a strong predilection for involvement of central digits of the hands and feet, with sparing of the thumb/great toe and small finger/toe. The average number of involved limbs per child was 2.6; 23% of the children had involvement of only 1 limb. Children wi …
There was a strong predilection for involvement of central digits of the hands and feet, with sparing of the thumb/great toe and smal …
Toe syndactyly revisited.
Marsh DJ, Floyd D. Marsh DJ, et al. J Plast Reconstr Aesthet Surg. 2011 Apr;64(4):535-40. doi: 10.1016/j.bjps.2010.07.016. Epub 2010 Aug 14. J Plast Reconstr Aesthet Surg. 2011. PMID: 20708986
INTRODUCTION: Toe syndactyly affects around 1/2000 people and is associated with significant psychological morbidity. There are multiple techniques of toe syndactyly repair described in the literature which is indicative that as yet, no one method has …
INTRODUCTION: Toe syndactyly affects around 1/2000 people and is associated with significant psychological morbidity. There ar …
Carrier frequency and incidence estimation of Smith-Lemli-Opitz syndrome in East Asian populations by Genome Aggregation Database (gnomAD) based analysis.
Park JE, Lee T, Ha K, Ki CS. Park JE, et al. Orphanet J Rare Dis. 2021 Apr 9;16(1):166. doi: 10.1186/s13023-021-01789-2. Orphanet J Rare Dis. 2021. PMID: 33836803 Free PMC article.
BACKGROUND: Smith-Lemli-Opitz syndrome (SLOS) is an autosomal, recessively inherited congenital malformation syndrome characterized by multiple congenital anomalies such as microcephaly with mental defects, distinctive facial features, genital abnormalities, and 2-3 syndactyly …
BACKGROUND: Smith-Lemli-Opitz syndrome (SLOS) is an autosomal, recessively inherited congenital malformation syndrome characterized by multi …