2024/2/6 -Pathology. Subtypes. Chondrodysplasia punctata can be broadly divided into rhizomelic and non-rhizomelic forms: rhizomelic chondrodysplasia punctata (RCDP).
2024/4/10 -Disease definition. Rhizomelic syndrome, Urbach type is a rare primary bone dysplasia characterized by upper limbs rhizomelia and other skeletal anomalies ...
2024/2/28 -Rhizomelic limb shortening with dysmorphic features (RLSDF) is characterized by rhizomelic shortening of the extremities, predominantly of the upper limbs, and ...
2024/5/14 -Rhizomelic dwarfism is a bone dysplasia that presents with a greater biometric reduction in rhizomelic structures, which are those more proximal to the ...
2024/4/10 -This disease is described under Rhizomelic chondrodysplasia punctata. Detailed information. General public. Article for general public.
2023/12/19 -Rhizomelic Chondrodysplasia Punctata is a rare inherited condition that affects fewer than 1 in 100,000 people worldwide. RCP type 1 is more common than RCP ...
2024/1/29 -Patients present with rhizomelic dwarfism, lumbar and foramen magnum stenosis, frontal bossing, and normal intelligence. Diagnosis is usually made based on ...
2024/3/21 -Rhizomelic Chondrodysplasia Punctata. Symptoms of rhizomelic chondrodysplasia punctata begin in infancy and include a sunken appearance of the middle of the ...
2023/12/8 -... (rhizomelic shortening), and macrocephaly. Patients with achondroplasia may have delayed motor development early on, but cognition is normal. There are a ...