Preface

Jarind's Letters

Sims'Letters

Genetic Lists

Prevention

Letters of Signs

Genetic Lists of Abnormal Genes ( Lists of Sims' Letters)

 

W = Musculoskeletal & Connective tissue

Achondroplasia

W1 = Achondroplasia autosomal dominant
(Classical chondrodystrophy)
w2 = Arthrogryposis multiplex congenita
(Amyoplasia congenita)
W3,w3 = Charcot-Marie-Tooth peroneal muscular atrophy
autosomal dominant & autosomal recessive
w4 = Chondroectodermal dysplasia autosomal recessive
(Ellis-Van Creveld syndrome)
W5 = Distal myopathies autosomal dominant
Gowers' type(Wasting of cranial musculature)
Welander's(Weakness of hands and feet)
w6 = Limb-girdle muscular dystrophy autosomal recessive
Pelvifemoral(Leydon-Mobius,)
Scapulohumeral(Erb's juvenile)
W7 = Muscular dystrophy autosomal dominant
(Facioscapulohumeral syndrome of Landouzy-Dejerine)
W8 = Myotonia atrophica autosomal dominant
(Myotonic dystrophy, Steinert's disease)
W9 = Myotonia congenita autosomal dominant
(Thomsen's disease)
w10 = Obesity in Familial hypoglycemosis
w11 = Obesity in Gycogen storage disease
w12 = Obesity in Laurence-Moon-Bardet-Biedl syndrome
autosomal recessive
W13 = Obesity in Prader-Willi syndrome
W14 = Osteogenesis imperfecta
(autosomal dominant mutant gene)
w15 = Osteopetrosis
(Albers-Schonberg,Marble bones disease)
W16 = Periodic paralysis autosomal dominant
(Hyperkalemic type)
W17 = Periodic paralysis autosomal dominant
(Hypokalemic type)
W18 = Periodic paralysis autosomal dominant
(Normokalemic type)
W19 = Progressive dystrophia ophthalmoplegica
( autosomal dominant )
w20 = Progressive muscular dystrophy X-linked recessive
(Tardive type of Becker)
w21 = Progressive systemic sclerosis X-linked recessive
(Polyarthralgia,Scleroderma)
w22 = Pseudohypoparathyroidism X-linked recessive
w23 = Severe generalized familial muscular dystrophy
(Duchenne's pseudohypertrophic muscular dystrophy)
X-linked recessive
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Update since 16/09/50