Acromesomelic Dysplasia Campailla Martinelli Type Latest Advances
Find the Latest Research About Acromesomelic Dysplasia Campailla Martinelli Type
Last Updated: 06/30/2026
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Found 923 publications
Acromelic dysplasias: similarities and differences in clinical and molecular findings in 12 Turkish patients.
Journal: European journal of pediatrics
Published: March 27, 2026
A Male Infant With Chondrodysplasia Punctata Presenting With Apnea and Growth Faltering: A Case Report.
Journal: Journal of paediatrics and child health
Published: March 12, 2026
A 12,000-Year-Old Case of NPR2-Related Acromesomelic Dysplasia.
Journal: The New England journal of medicine
Published: January 28, 2026
Ultrasound for evaluation of atlantoaxial instability in neonates with chondrodysplasia punctata.
Journal: Pediatrics and neonatology
Published: January 04, 2026
Neonatal X-linked recessive chondrodysplasia punctata.
Journal: QJM : monthly journal of the Association of Physicians
Published: October 20, 2025
Management of a geminated tooth and supernumeraries in a patient with Acromesomelic Dysplasia, Maroteaux type.
Journal: Journal of clinical orthodontics : JCO
Published: October 18, 2025
Fetal chondrodysplasia punctata: a clinical study of five cases.
Journal: American journal of translational research
Published: October 17, 2025
Clinical, Molecular Characteristics, and Genotype-Phenotype Relationships of Metaphyseal Chondrodysplasia Type Schmid.
Journal: Calcified tissue international
Published: October 06, 2025
Case Report: Dual pathogenic mechanism of a PRKG2 missense variant underlies an attenuated phenotype of acromesomelic dysplasia.
Journal: Frontiers in genetics
Published: September 19, 2025
A diagnostic and management odyssey of a rare case of rhizomelic chondrodysplasia punctata.
Journal: JPMA. The Journal of the Pakistan Medical Association
Published: August 25, 2025
Last Updated: 06/30/2026