Acromicric Dysplasia Latest Advances

Challenges Associated With First Web Space Congenital Syndactyly Reconstruction of the Hand.

Journal: Journal of hand surgery global online

Published: April 09, 2026

Ocular manifestations of Apert syndrome: a case report

Journal: [Zhonghua yan ke za zhi] Chinese journal of ophthalmology

Published: April 07, 2026

Predictors of early and late complications after syndactyly release: A retrospective review of 684 cases.

Journal: The Journal of hand surgery, European volume

Published: March 18, 2026

Congenital Upper Extremity Anomalies Misdiagnosed as Ulnar Longitudinal Deficiency.

Journal: Eplasty

Published: March 13, 2026

Syndactyly and Risk of Cancer.

Journal: Hand (New York, N.Y.)

Published: March 09, 2026

Genetic insights into syndromic anophthalmia/microphthalmia: novel molecular findings in a prenatal context.

Journal: Ophthalmic genetics

Published: March 08, 2026

Navigating challenges: a child with Apert syndrome and global developmental delay from a low-income family.

Journal: BMJ case reports

Published: March 05, 2026

Kikuchi Disease With Marfanoid Features in a Background of Fever of Unknown Origin.

Journal: Cureus

Published: February 22, 2026

Type I Thanatophoric Dysplasia: Clinical Outcome in the Absence of Molecular Genetic Confirmation: A Case Report.

Journal: Cureus

Published: February 18, 2026

Talocalcaneal Coalition: Current Concepts, Clinical Implications, and Management Strategies.

Journal: Life (Basel, Switzerland)

Published: February 11, 2026

ACR Appropriateness Criteria® Chronic Ankle Pain: Update 2025.

Journal: Journal of the American College of Radiology : JACR

Published: February 10, 2026

Clinical characteristics and prenatal diagnosis of a fetus with Short-rib thoracic dysplasia syndrome due to variants of DYNC2H1 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: February 06, 2026

Acromicric Dysplasia Latest Advances

Find the Latest Research About Acromicric Dysplasia

Challenges Associated With First Web Space Congenital Syndactyly Reconstruction of the Hand.

Challenges Associated With First Web Space Congenital Syndactyly Reconstruction of the Hand.

Ocular manifestations of Apert syndrome: a case report

Ocular manifestations of Apert syndrome: a case report

Predictors of early and late complications after syndactyly release: A retrospective review of 684 cases.

Predictors of early and late complications after syndactyly release: A retrospective review of 684 cases.

Congenital Upper Extremity Anomalies Misdiagnosed as Ulnar Longitudinal Deficiency.

Congenital Upper Extremity Anomalies Misdiagnosed as Ulnar Longitudinal Deficiency.

Syndactyly and Risk of Cancer.

Syndactyly and Risk of Cancer.

Genetic insights into syndromic anophthalmia/microphthalmia: novel molecular findings in a prenatal context.

Genetic insights into syndromic anophthalmia/microphthalmia: novel molecular findings in a prenatal context.

Navigating challenges: a child with Apert syndrome and global developmental delay from a low-income family.

Navigating challenges: a child with Apert syndrome and global developmental delay from a low-income family.

Kikuchi Disease With Marfanoid Features in a Background of Fever of Unknown Origin.

Kikuchi Disease With Marfanoid Features in a Background of Fever of Unknown Origin.

Type I Thanatophoric Dysplasia: Clinical Outcome in the Absence of Molecular Genetic Confirmation: A Case Report.

Type I Thanatophoric Dysplasia: Clinical Outcome in the Absence of Molecular Genetic Confirmation: A Case Report.

Talocalcaneal Coalition: Current Concepts, Clinical Implications, and Management Strategies.

Talocalcaneal Coalition: Current Concepts, Clinical Implications, and Management Strategies.

ACR Appropriateness Criteria® Chronic Ankle Pain: Update 2025.

ACR Appropriateness Criteria® Chronic Ankle Pain: Update 2025.

Clinical characteristics and prenatal diagnosis of a fetus with Short-rib thoracic dysplasia syndrome due to variants of DYNC2H1 gene

Clinical characteristics and prenatal diagnosis of a fetus with Short-rib thoracic dysplasia syndrome due to variants of DYNC2H1 gene