Facial dysmorphism, skeletal anomalies, congenital glucoma

Axenfeld–Rieger syndrome: orthopedic and orthodontic management in a pediatric patient: a case report, Head & Face Medicine

Frank-Ter Haar Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

Genes, Free Full-Text

rare_diseases_in_pediatric_anesthesia

Secondary Childhood glaucoma – a rare association in Seckel syndrome - Manju R Pillai, Srilekha Pallamparthy, Subathra Gnanavelu, 2023

Patient 3. (A) Facial dysmorphism: short palpebral fissures, short

Secondary Childhood glaucoma – a rare association in Seckel syndrome - Manju R Pillai, Srilekha Pallamparthy, Subathra Gnanavelu, 2023

Hallermann Streiff Syndrome - an overview

PDF] Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome

Two novel GJA1 variants in oculodentodigital dysplasia - Pace - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Mild facial dysmorphism. Noticeable long eyelashes, bulbous nose, and