File:Smith‐Lemli‐Opitz syndrome phenotype.jpg
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Summary
| Description |
English: The features of the proband, at 18‐24 months old, include down‐slanting palpebral fissures, slightly low‐set and prominent ears, bilateral transverse creases, pectus excavatum and bilateral two to three toes syndactyly |
| Date | |
| Source | "Familial DHCR7 genotype presenting as a very mild form of Smith‐Lemli‐Opitz syndrome and lethal holoprosencephaly" (Temple et al., 2020) |
| Author | Suzanna E. L. Temple, Rani Sachdev, and Carolyn Ellaway |
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 11:55, 14 September 2022 | | 709 × 520 (115 KB) | CopperKettle | Uploaded a work by Suzanna E. L. Temple, Rani Sachdev, and Carolyn Ellaway from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653247/ "Familial DHCR7 genotype presenting as a very mild form of Smith‐Lemli‐Opitz syndrome and lethal holoprosencephaly" (Temple et al., 2020) with UploadWizard |
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