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Differential Diagnosis For Short stature: Congenital, Developmental Disorders

List of current finding(s):

Congenital, Developmental Disorders: next: Genetic Causes: Congenital disorders; Down's Syndrome; CHARGE Congenital syndrome; Adrenogenital syndrome; Congenital acyanotic heart disease; Congenital cyanotic heart disease; Congenital heart disease; Congenital syndromes; Cretinism, goitrous sporadic; Hip osteochondrosis/capital epiphysitis/LCP Dis; Placenta insufficiency syndrome/infant; Renal tubular acidosis; Renal tubular acidosis, proximal/type 2; Chondrodystrophy; Cirrhosis, congenital/neonatal; Cretinism; Cri du Chat/Chromosome 5p (5p15.2); Distal renal tubular acidosis/type 1; Dwarf; Dysplasia, chondroectodermal; Dysplasia, multiple epiphyseal; Epiphysis long bones/premature closure; Nephrogenic diabetes insipidus; Trisomy-21 partial translocation; Turner syndrome/Gonadal dysgenesis; Mulibrey Nanism syndrome; Achondrogenesis; Achondroplasia; Adiposogenital dystrophy; Agammaglobulinemia, congenital/autosomal; Anetoderma/osteogenesis imperfecta (Blegvad-Haxthausen); Arthrogryposis, multiplex, congenita; Asphyxiating thoracic dysplasia/Jeune; Bloom syndrome; Campomelic dwarfism; Chondroectodermal dysp.(Ellis-Van Crev); Chromosome 4p-syndrome; Chromosome XXXXX Syndrome; Craniocarpotarsal Dystrophy (Freeman Sheldon); Craniofacial dysostosis/Crouzon; De Lange syndrome; Diastrophic dwarfism; Dubowitz syndrome; Dwarfism, ateliotic; Dysostosis multiplex; Dysplasia, asphyxiating thoracic; Dysplasia, epiphyseal hemimelica; Hallermann-Streiff-Francois syndrome; Jansen's metaphyseal chondrodysplasia (unco); King Syndrome; Laron dwarfism/GH receptor defect; Larsen Dysmorphic Syndrome; Noonan syndrome; Parastremmatic dwarfism; Polyostotic fibrous dysplasia (MAS syn); Prader-Willi syndrome; Progeria; Progeria of child (Hutchinson-Gilford); Progeria/adult (Werners syndrome); Renpennings's syndrome; Robinow dwarfing syndrome/mesomelic dys; Rubinstein-Taybi syndrome; Septo-optic Dysplasia (DeMorsier); Shawl scrotum syndrome; Silver-Russell syndrome; Singleton-Merten syndrome; Smith Magenis syndrome; Thanatophoric dwarfism; Triple X/Chromosome syndrome (XXX dis); Trisomy-18 syndrome; Turner mosaic syndrome; Velocardiofacial (22q gene) syndrome; Weismann-Netter-Stuhl syndrome; Coffin-Lowry Syndrome; Cohen Syndrome; Grebe Syndrome; Metatropic dwarfism (Kneist Dysplasia); Porteous Syndrome

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