Phenotype #0000309917

Individual ID 00418581
Associated disease ?
Diagnosis/Initial brachyolmia, mucopolysaccharidosis, spondyloepiphysial dysplasia
Diagnosis/Definite MPS10
Phenotype details height 157 cm, -3.22 SD, OFC 53 cm, -2.21 SD; coarse facial features, long philtrum, broad nasal root; normal eyes; normal auditory system; normal jaw, normal teeth; normal habds/wrists; disproportionate short-trunk short stature, genu valgus; liver normal; spleen normal; ; heart normal; neurological examination normal; thickened cortical bone calvaria; no rounded or bullet-shape vertebral bodies; irregular vertebral end plates; platyspondyly; anterior inferior beaking thoracolumbar vertebrae; posterior scalloping vertebral bodies; no thoracolumbar junction kyphosis; no kyphosis with gibbus; hyperlordosis; no scoliosis; no spinal cord compression; poor development acetabulum and medial proportion of proximal femoral epiphysis; iregular acetabular roofs, reduced hip joint space; severe hip dysplasia; carpal and tarsal bones hypoplastic and irregularly shaped; metacarpal bones proximally pointed, shortened and thickened; short third, fourth and fifth metacarpals; hypoplastic and thinned epiphyses cortically with osteoporosis; small epiphyses of lower ends of radius, ulna and capital femur; metaphyseal striae; abnormally shaped ribs, spatulate ribs, broadening of clavicles and ribs
Inheritance Familial, autosomal recessive
Age/Examination 18y (18 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-09-30 11:29:08 +02:00 (CEST)
Date last edited N/A

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