Laurin-Sandrow Syndrome (LSS)

Laurin-Sandrow Syndrome(来自ICD-11)

别称:

Sandrow Syndrome

Tetramelic Mirror-Image Polydactyly

Mirror-Image Polydactyly

Mirror Hands and Feets-Nasal Defects Syndrome

Tmip

Mirror Hands and Feet with Nasal Defects

Lss

Mip

Fibula and Ulna, Duplication of, with Absence of Tibia and Radius

Mipduplication of Fibuland Ulna with Absence of Tibia and Radius

Duplication of Fibula and Ulna with Absence of Tibia and Radius

Miccor Hands and Feet with Nasal Defects

Laurin-Sandrow Syndrome, Segmental

Segmental Laurin-Sandrow Syndrome

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Laurin-Sandrow Syndrome, also known as sandrow syndrome, is related to triphalangeal thumb with polysyndactyly and clubfoot. An important gene associated with Laurin-Sandrow Syndrome is LMBR1 (Limb Development Membrane Protein 1), and among its related pathways/superpathways are Signaling by Hedgehog and Bardet-Biedl syndrome. Affiliated tissues include bone and thymus, and related phenotypes are preaxial hand polydactyly and finger syndactyly

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