Cleidocranial Dysplasia Latest Advances

Inherited Retinal Dystrophy in an 11-month-old Infant with Yunis-Varon Syndrome and Homozygous FIG4 Mutation.

Journal: Retinal cases & brief reports

Published: August 14, 2026

Incidental Isolated Bilateral Clavicular Agenesis Discovered During Preoperative Hernia Assessment of a 78-Year-Old Male in Rural Uganda: A Case Report.

Journal: International medical case reports journal

Published: May 28, 2026

A Novel 4.2 kb deletion of the 3'UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3'UTR.

Journal: Balkan journal of medical genetics : BJMG

Published: May 18, 2026

Optimized Approach for Retrieval of Multiple Impacted Teeth in Cleidocranial Dysplasia.

Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association

Published: May 15, 2026

Cleidocranial dysplasia caused by a novel de novo RUNX2 splice-site variant.

Journal: Human genome variation

Published: April 21, 2026

Cleidocranial dysplasia with preserved function under conservative management: a case report.

Journal: Frontiers in pediatrics

Published: March 31, 2026

The vascular-osteogenic interface in craniofacial development: a structured review of emerging associations in congenital malformations.

Journal: Developmental biology

Published: March 02, 2026

Clinical and immunological features of a patient exhibiting delayed puberty, microcephaly, scoliosis and epilepsy caused by a novel mutation in IGSF10.

Journal: Frontiers in cell and developmental biology

Published: February 25, 2026

Cleidocranial dysplasia with complex oral manifestations: a case report.

Journal: BMC oral health

Published: February 17, 2026

Sost deficiency restores calvarial bone thickness without recovery of sutural growth in Runx2 missense mutant mice.

Journal: Biochemical and biophysical research communications

Published: February 06, 2026

Early prenatal detection of autosomal dominant skeletal dysplasia using first-trimester ultrasound and cell-free fetal DNA screening: three case reports.

Journal: Hong Kong medical journal = Xianggang yi xue za zhi

Published: January 27, 2026

Deep-Intronic Variant in RUNX2 Causing Pseudo-Exon Inclusion in a Family With Cleidocranial Dysplasia.

Journal: Clinical genetics

Published: January 12, 2026

Cleidocranial Dysplasia Latest Advances

Find the Latest Research About Cleidocranial Dysplasia

Inherited Retinal Dystrophy in an 11-month-old Infant with Yunis-Varon Syndrome and Homozygous FIG4 Mutation.

Inherited Retinal Dystrophy in an 11-month-old Infant with Yunis-Varon Syndrome and Homozygous FIG4 Mutation.

Incidental Isolated Bilateral Clavicular Agenesis Discovered During Preoperative Hernia Assessment of a 78-Year-Old Male in Rural Uganda: A Case Report.

Incidental Isolated Bilateral Clavicular Agenesis Discovered During Preoperative Hernia Assessment of a 78-Year-Old Male in Rural Uganda: A Case Report.

A Novel 4.2 kb deletion of the 3'UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3'UTR.

A Novel 4.2 kb deletion of the 3'UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3'UTR.

Optimized Approach for Retrieval of Multiple Impacted Teeth in Cleidocranial Dysplasia.

Optimized Approach for Retrieval of Multiple Impacted Teeth in Cleidocranial Dysplasia.

Cleidocranial dysplasia caused by a novel de novo RUNX2 splice-site variant.

Cleidocranial dysplasia caused by a novel de novo RUNX2 splice-site variant.

Cleidocranial dysplasia with preserved function under conservative management: a case report.

Cleidocranial dysplasia with preserved function under conservative management: a case report.

The vascular-osteogenic interface in craniofacial development: a structured review of emerging associations in congenital malformations.

The vascular-osteogenic interface in craniofacial development: a structured review of emerging associations in congenital malformations.

Clinical and immunological features of a patient exhibiting delayed puberty, microcephaly, scoliosis and epilepsy caused by a novel mutation in IGSF10.

Clinical and immunological features of a patient exhibiting delayed puberty, microcephaly, scoliosis and epilepsy caused by a novel mutation in IGSF10.

Cleidocranial dysplasia with complex oral manifestations: a case report.

Cleidocranial dysplasia with complex oral manifestations: a case report.

Sost deficiency restores calvarial bone thickness without recovery of sutural growth in Runx2 missense mutant mice.

Sost deficiency restores calvarial bone thickness without recovery of sutural growth in Runx2 missense mutant mice.

Early prenatal detection of autosomal dominant skeletal dysplasia using first-trimester ultrasound and cell-free fetal DNA screening: three case reports.

Early prenatal detection of autosomal dominant skeletal dysplasia using first-trimester ultrasound and cell-free fetal DNA screening: three case reports.

Deep-Intronic Variant in RUNX2 Causing Pseudo-Exon Inclusion in a Family With Cleidocranial Dysplasia.

Deep-Intronic Variant in RUNX2 Causing Pseudo-Exon Inclusion in a Family With Cleidocranial Dysplasia.