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Differential Diagnosis For Short stature Child: Congenital, Developmental Disorders
List of current finding(s):
Short stature Child
- Infectious Disorders (Specific Agent) (10)
- Infected organ, Abscesses (4)
- Neoplastic Disorders (1)
- Allergic, Collagen, Auto-Immune Disorders (9)
- Metabolic, Storage Disorders (32)
- Deficiency Disorders (11)
- Congenital, Developmental Disorders (64)
- Hereditary, Familial, Genetic Disorders (59)
- Usage, Degenerative, Necrosis, Age Related Disorders (2)
- Relational, Mental, Psychiatric Disorders (2)
- Functional, Physiologic Variant Disorders (2)
- Vegetative, Autonomic, Endocrine Disorders (12)
- Reference to Organ System (10)
- Idiopathic, Unclassified Disorders (1)
- Drugs (2)
- Poisoning (Specific Agent) (2)
- Synonyms (15)
- Definition
- External Links Related to Short stature Child
- Congenital, Developmental Disorders:
- Congenital disorders
- Down's Syndrome
- CHARGE Congenital syndrome
- Adrenogenital syndrome
- Congenital acyanotic heart disease
- Congenital cyanotic heart disease
- Congenital heart disease
- 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
- Cretinism
- Cri du Chat/Chromosome 5p (5p15.2)
- Dwarf
- Nephrogenic diabetes insipidus
- Trisomy-21 partial translocation
- Turner syndrome/Gonadal dysgenesis
- Mulibrey Nanism syndrome
- Achondrogenesis
- Achondroplasia
- Agammaglobulinemia, congenital/autosomal
- Anetoderma/osteogenesis imperfecta (Blegvad-Haxthausen)
- Arthrogryposis, multiplex, congenita
- Asphyxiating thoracic dysplasia/Jeune
- Bloom syndrome
- Campomelic dwarfism
- Chromosome 4p-syndrome
- Chromosome XXXXX Syndrome
- Craniocarpotarsal Dystrophy (Freeman Sheldon)
- Craniofacial dysostosis/Crouzon
- De Lange syndrome
- Diastrophic dwarfism
- Dubowitz syndrome
- Dwarfism, ateliotic
- Hallermann-Streiff-Francois syndrome
- Jansen's metaphyseal chondrodysplasia (unco)
- 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)
- 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
- CODAS Syndrome
- Coffin-Lowry Syndrome
- Cohen Syndrome
- Metatropic dwarfism (Kneist Dysplasia)
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© 2013 MedTech USA, Inc. (last modified on 06/19/13)
