Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation.

Abstract

BACKGROUND:

The kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA) (OMIM 225400) is a rare inheritable connective tissue disorder characterized by a deficiency of collagen lysyl hydroxylase 1 (LH1; EC 1.14.11.4) due to mutations in PLOD1. Biochemically this results in underhydroxylation of collagen lysyl residues and, hence, an abnormal pattern of lysyl pyridinoline (LP) and hydroxylysyl pyridinoline (HP) crosslinks excreted in the urine. Clinically the disorder is characterized by hypotonia and kyphoscoliosis at birth, joint hypermobility, and skin hyperelasticity and fragility. Severe hypotonia usually leads to delay in gross motor development, whereas cognitive development is reported to be normal.

METHODS:

We describe the clinical, biochemical and molecular characterisation, as well as electron microscopy findings of skin, in 15 patients newly diagnosed with this rare type of Ehlers-Danlos syndrome.

RESULTS:

Age at diagnosis ranged from 5 months to 27 years, with only 1/3 of the patients been diagnosed correctly in the first year of life. A similar disease frequency was found in females and males, however a broad disease severity spectrum (intra- and interfamilial), independent of molecular background or biochemical phenotype, was observed. Kyphoscoliosis, one of the main clinical features was not present at birth in 4 patients. Importantly we also noted the occurrence of vascular rupture antenatally and postnatally, as well as developmental delay in 5 patients.

CONCLUSION:

In view of these findings we propose that EDS VIA is a highly variable clinical entity, presenting with a broad clinical spectrum, which may also be associated with cognitive delay and an increased risk for vascular events. Genotype/phenotype association studies and additional molecular investigations in more extended EDS VIA populations will be necessary to further elucidate the cause of the variability of the disease severity.

• Authors: Marianne Rohrbach, Anthony Vandersteen, Uluç Yiş, Gul Serdaroglu, Esra Ataman, Maya Chopra, Sixto Garcia, Kristi Jones, Ariana Kariminejad, Marius Kraenzlin, Carlo Marcelis, Matthias Baumgartner, Cecilia Giunta
• Journal: Orphanet journal of rare diseases (Orphanet J Rare Dis) Vol. 6 Pg. 46 (Jun 23 2011) ISSN: 1750-1172 [Electronic] England
• PMID: 21699693 (Publication Type: Journal Article)

Chemical References

• Amino Acids
• pyridinoline
• Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase

Topics

• Adolescent
• Adult
• Amino Acids (urine)
• Biopsy
• Cells, Cultured
• Child
• Child, Preschool
• DNA Mutational Analysis
• Developmental Disabilities (genetics, pathology)
• Ehlers-Danlos Syndrome (diagnosis, genetics, pathology)
• Female
• Fibroblasts (pathology)
• Genotype
• Humans
• Infant
• Kyphosis (genetics, pathology)
• Male
• Muscle Hypotonia (genetics, pathology)
• Phenotype
• Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase (genetics)
• Scoliosis (genetics, pathology)
• Skin (pathology)