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449 Possible Causes for Syndactyly of Toes 2-3

  • Smith Lemli Opitz Syndrome

    3 syndactyly of the toes.[ncbi.nlm.nih.gov] In this report we describe a male newborn with trisomy 13 who also has features of SLOS, such as 2/3 toe syndactyly and a shawl-like scrotum.[ncbi.nlm.nih.gov] The SLOS was confirmed in only five Arab patients with growth retardation, global developmental delay, dysmorphic features, and 2-3 toe syndactyly, among other findings.[ncbi.nlm.nih.gov]

  • Growth Failure

    9.6 6.2 Mild None (1.23) (37) (65) F9 M 37 1.4 1.6 5y6m 10.8 2.9 Mild Hypopigmentation, hypermobile knees, single palmar crease, 2/3 toe syndactyly, sandal gap (2.25) (30.8[ncbi.nlm.nih.gov] 3 toe syndactyly, excessive vomiting (gastrostomy in situ) (0.95) (27) (36.5) (75) F7 F 37 4.1 4.21 3y8m 10.03 5.15 None None (1.29) (27.5) (38.8) (79) F8 F 34 2.93 N/A 1y9m[ncbi.nlm.nih.gov] ) (39) (98) F10 M 37 4.0 5.33 3m 10.1 8.4 N/A Pre-axial polydactyly 2/5 toe syndactyly, dysplastic kidney and dysgenesis of corpus callosum. (1.3) (26.5) (29) (43) Facial[ncbi.nlm.nih.gov]

  • Syndactyly

    1-3 toe syndactyly 1-5 finger complete cutaneous syndactyly 2-3 finger syndactyly 2-3 toe cutaneous syndactyly 2-3 toe syndactyly 2-4 finger syndactyly 2-4 toe cutaneous[mousephenotype.org] Image 1. 3 cases of syndactyly between 2 and 3 toes. Image 5. 2 cases of syndactyly between 1 and 2 toes.[en.atlaseclamc.org] 3 and 4 or toes 2 and 3 Can be bilateral in hands (50%) and feet (66%) Syndactyly of toes is four times more common than fingers Can be inherited as autosomal dominant trait[en.wikibooks.org]

  • Epilepsy

    […] of toes 2 and 3 Other features Mild thoracic scoliosis Reduced body fat mass Strabismus Mild thoracic scoliosis Strabismus PIP joint fusion of thumbs Mild peripheral hearing[doi.org] She had mild thoracic scoliosis, fusion of the proximal interphalangeal joint in both thumbs, bilateral fifth-finger brachydactyly, tapered fingers and cutaneous 2-3 syndactyly[doi.org] […] of the toes.[doi.org]

  • Saethre-Chotzen Syndrome

    […] valgus, bilateral symmetrical complete soft tissue syndactyly of toes 2 and 3, and partial soft tissue syndactyly of toes 4 and 5 consistent with the diagnosis of Saethre-Chotzen[ncbi.nlm.nih.gov] […] hallux valgus, bilateral symmetrical complete soft tissue syndactyly of toes 2 and 3, and partial soft tissue syndactyly of toes 4 and 5 consistent with the diagnosis of[unboundmedicine.com] […] of fingers 2-3 and toes 3-4; autosomal dominant inheritance, caused by mutation in the TWIST transcription factor gene on chromosome 7p.[medical-dictionary.thefreedictionary.com]

  • Cardiodysrhythmic Potassium-Sensitive Periodic Paralysis

    Figure (A) Fifth digit clinodactyly and (B) syndactyly of the toes 2 and 3, highly suggestive of Andersen-Tawil syndrome.[scielo.br] […] of toes 2 and 3 B.[ncbi.nlm.nih.gov] […] of the following: ‐ Low‐set ears ‐ Widely spaced eyes ‐ Small mandible ‐ Fifth‐digit clinodactyly ‐ Syndactyly of toes 2 and 3 B. [doi.org]

  • Popliteal Pterygium Syndrome

    Syndactyly of toes 2/3 and partial syndactyly of toes 3/4 was noted.[jmg.bmj.com] 2-3 toe syndactyly.[docslide.com.br] He also had right popliteal pterygium and bilateral syndactyly of four to five toes (Figure 3 ). The urogenital examination showed a phimosis.[jmedicalcasereports.biomedcentral.com]

  • Esotropia

    3 toe syndactyly Areflexia Decreased motor nerve conduction velocity Cerebral dysmyelination Clitoral hypertrophy Decreased nerve conduction velocity Hoarse cry Progressive[mendelian.co] […] nerve hypoplasia Abnormality of mitochondrial metabolism Aqueductal stenosis Partial agenesis of the corpus callosum Low-set ears Nonketotic hyperglycinemia Gait disturbance 2-[mendelian.co]

  • Brachydactyly

    […] thumbs, and cutaneous syndactyly of toes 2 and 3.[malacards.org] His right foot had a short, dorsiflexed hallux with a hypoplastic nail, 2-3 syndactyly and an overlapping toe.[ncbi.nlm.nih.gov] The limb phenotypes observed in this syndrome overlap those of brachydactyly types A4, D, E and syndactyly type 1.[malacards.org]

  • Bjornstad Syndrome

    OBSL1 Three M syndrome type 3 CCDC8 Toe syndactyly, telecanthus, and anogenital and renal malformations FAM58A Tooth agenesis, selective type 1 MSX1 Tooth agenesis, selective[centogene.com] […] syndrome maternal UPD chr. 14 Temple-Baraitser syndrome KCNH1 Temtamy syndrome C12orf57 Tetraamelia, autosomal recessive WNT3 Three M syndrome type 1 CUL7 Three M syndrome type 2[centogene.com]

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