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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Dr.Jarind B. Sriraumpuch |
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Update since 16/09/50