Developmental Foot Deformities in Patients with Connective T... : JBJS Reviews
Developmental Foot Deformities in Patients with Connective Tissue Disorders : JBJS …

Skeletal dysplasias or osteochondrodysplasias comprise a large heterogeneous group of
genetic disorders and possess significant overlap on imaging, which adds to the dilemma of …

Hereditary connective tissue disorders have overlapping phenotypes, particularly in regard
to musculoskeletal features. This contributes to the challenge of phenotype-based clinical …

Background: The limited understanding of human inner ear pathologies and their associated
biomolecular variations hinder efforts to develop disease-specific diagnostics and …

Larsen syndrome is a rare genetic disorder characterized by weak connective tissues and
various musculoskeletal abnormalities. This is a case report of a 39-year-old patient with …

Larsen syndrome is a rare genetic disorder that affects the connective tissue within the body.
The present narrative review aims to examine the genetic basis of Larsen syndrome, clarify …

Aufgrund der Heterogenität der Erkrankung ist das Erstellen einer Klassifikation schwer,
jedoch notwendig, um eine gemeinsame wissenschaftliche Basis zu definieren. Erstmalig …

Larsen syndrome is a muscle biopsy negative complex genetic syndrome with characteristic
flat facies, wide-set eyes, and multiple congenital joint dislocations (shoulder, elbow, hip …

Larsen Syndrome (LS) is a rare genetic disorder of osteochondrodysplasia and was first
described by Larsen in 1950 [1]. LS is genetically heterogeneous and consists of an …

Hintergrund Skelettdysplasien beinhalten eine inhomogene Gruppe an Erkrankungen des
Knochens, Knorpels und Bindegewebes. Deletionen im Gen für das Filamin B-Protein …