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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
Cirrhosis, congenital/neonatal
Cri du Chat/Chromosome 5p (5p15.2)
Distal renal tubular acidosis/type 1
Dysplasia, chondroectodermal
Dysplasia, multiple epiphyseal
Epiphysis long bones/premature closure
Nephrogenic diabetes insipidus
Trisomy-21 partial translocation
Turner syndrome/Gonadal dysgenesis
Mulibrey Nanism syndrome
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 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