Trichorhinophalangeal syndrome (TRPS), a type of skeletal dysplasia, is characterized by a triad of dysmorphic (bulbous nose and large ears); ectodermal (thin and sparse hair); and skeletal (short stature and cone-shaped epiphyses) findings, and this combination is helpful for early diagnosis and appropriate follow-up. A 14-year-old boy presented with short stature and distinctive facial features, and following the first clinical and biological evaluation, no precise diagnosis was reached. Progressive bilateral development of noninflammatory and painless deformity of his second finger required a radiological exam that highlighted the key elements (cone-shaped epiphyses) for final diagnosis. This case illustrates the difficulties to early re...
Tricho-rhino-phalangeal syndrome type I (TRPS I) is characterized by a bulbous nose, sparse hair and...
Tricho-rhion-phalangeal syndrome is characterized by the triad of slow growing, brittle hair and ear...
We report a boy with SHORT syndrome with distinctive radiographic features, comprising large epiphys...
Abstract Background Trichorhinophalangeal syndrome (TRPS) is a rare autosomal dominant disorder caus...
Tricho-rhino-phalangeal syndrome (TRPS) is a genetic disease characterized by craniofacial and skele...
We report a 4.5 year old Egyptian male child, fourth in the order of birth of healthy remote consang...
AbstractWe report a 4.5year old Egyptian male child, fourth in the order of birth of healthy remote ...
AbstractThe tricho-rhino-phalangeal syndrome (TRPS) type I is a rare genetic disorder related to the...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
Skeletal dysplasias are conditions in which there is an abnormality of bone and/or cartilage growth...
Tricho-rhino-phalangeal syndrome (TRPS) is characterized by craniofacial and skeletal abnormalities,...
Trichorhinophalangeal syndrome (TRPS) is the collective name of three rare congenital conditions cha...
A 14-year-old boy presented with proportionate short stature (height 140 cm; Upper segment: Lower se...
A 14-year-old boy presented with proportionate short stature (height 140 cm; Upper segment: Lower se...
Trichorhinophalangeal syndrome type I (TRPS I; MIM 190350) is a rare autosomal dominant disorder of ...
Tricho-rhino-phalangeal syndrome type I (TRPS I) is characterized by a bulbous nose, sparse hair and...
Tricho-rhion-phalangeal syndrome is characterized by the triad of slow growing, brittle hair and ear...
We report a boy with SHORT syndrome with distinctive radiographic features, comprising large epiphys...
Abstract Background Trichorhinophalangeal syndrome (TRPS) is a rare autosomal dominant disorder caus...
Tricho-rhino-phalangeal syndrome (TRPS) is a genetic disease characterized by craniofacial and skele...
We report a 4.5 year old Egyptian male child, fourth in the order of birth of healthy remote consang...
AbstractWe report a 4.5year old Egyptian male child, fourth in the order of birth of healthy remote ...
AbstractThe tricho-rhino-phalangeal syndrome (TRPS) type I is a rare genetic disorder related to the...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
Skeletal dysplasias are conditions in which there is an abnormality of bone and/or cartilage growth...
Tricho-rhino-phalangeal syndrome (TRPS) is characterized by craniofacial and skeletal abnormalities,...
Trichorhinophalangeal syndrome (TRPS) is the collective name of three rare congenital conditions cha...
A 14-year-old boy presented with proportionate short stature (height 140 cm; Upper segment: Lower se...
A 14-year-old boy presented with proportionate short stature (height 140 cm; Upper segment: Lower se...
Trichorhinophalangeal syndrome type I (TRPS I; MIM 190350) is a rare autosomal dominant disorder of ...
Tricho-rhino-phalangeal syndrome type I (TRPS I) is characterized by a bulbous nose, sparse hair and...
Tricho-rhion-phalangeal syndrome is characterized by the triad of slow growing, brittle hair and ear...
We report a boy with SHORT syndrome with distinctive radiographic features, comprising large epiphys...