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Differential Diagnosis For Prader-Willi syndrome - Rule Outs, Family history/Dwarfism
List of current finding(s):
Prader-Willi syndrome - Rule Outs
Family history/Dwarfism
- Metabolic, Storage Disorders
- Renal tubular disorders/metabolic
- Mucopolysaccharidoses
- Hurler's mucopolysaccharidosis syndrome
- Renal tubular acidosis type IV
- Gangliosidosis, generalized (GM1)
- Hunter's mucopolysaccharidosis syndrome
- Hurler-Scheie compound syndrome/mucopol
- Maroteaux-Lamy Mucopolysaccharidosis VI Syndrome
- Morquio's mucopolysaccharidosis synd.
- Sanfilippo's mucopolysaccharidosis synd
- Scheie syndrome
- Tryptophanemia
- Congenital, Developmental Disorders
- Renal tubular acidosis
- Renal tubular acidosis, proximal/type 2
- Mulibrey Nanism syndrome
- Achondrogenesis
- Achondroplasia
- Anetoderma/osteogenesis imperfecta (Blegvad-Haxthausen)
- Metatropic dwarfism (Kneist Dysplasia)
- Hereditary, Familial, Genetic Disorders
- Achondrogenesis I/Parenti-Fraccaro
- Osteogenesis imperfecta
- Pseudo-pseudohypoparathyroidism
- Johanson Blizzard genetic syndrome (unco)
- Pseudohypoparathyroidism
- Weill-Marchesani syndrome
- Achondrogenesis II/Langer-Saldino
- Bird-headed dwarf of Seckel
- Cockayne syndrome
- Dolichospondylic dysplasia
- Laurence-Moon-Biedel syndrome
- Metaphyseal chondrodysplasia
- Schwartz-Jampel syndrome
- Scott's Craniodigital syndrome
- Shwachman (Shwachman-Diamond) syndrome
- Sjogren-Larsson syndrome
- Smith-Lemli-Opitz syndrome
- Spondylometaphyseal dysplasia syndrome
- Williams syndrome/Elfin facies
- Vegetative, Autonomic, Endocrine Disorders
- Dwarfism, pituitary
- Reference to Organ System
- Renal osteodystrophy
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© 2013 MedTech USA, Inc. (last modified on 06/19/13)
