Associations

• Acrodysostosis

• Acromesomelic dysplasias

• Aplasia cutis congenita

• Arthritides

• Atelosteogenesis

• Beckwith-Wiedemann syndrome

• Biemond syndrome I

• Brachydactyly type E/atrial defect type II

• Brachydactyly, type E, with short stature and hypertension (Bilginturan syndrome)

• Brachymetapody-anodontia-hypotrichosis-albinoidism (Tuomaala syndrome)

• Camptobrachydactyly

• Cephaloskeletal dysplasia (Taybi-Linder syndrome)

• Cheirolumbar dysostosis

• Chondrodysplasia punctata

• Chromosome 18 trisomy syndrome

• Chromosome 5p- deletion syndrome

• Cockayne syndrome

• Cohen syndrome

• Cryptodontic metacarpalia

• C Syndrome (Opitz trigonocephaly syndrome)

• De Lange syndrome

• Deafness and metaphyseal dysostosis

• Diastrophic dysplasia

• Dyggve-Melchior-Clausen syndrome

• Dyschondrosteosis

• Dyssegmental dwarfism

• Enchondromatosis (Ollier disease)

• Exostoses/anetodermia/brachydactyly type E

• Fanconi anemia

• Fetal alcohol syndrome

• Fibrodysplasia ossificans progressiva

• Grebe chondrodysplasia

• Hand-foot-genital syndrome

• Holt-Oram syndrome

• Hypoparathyroidism

• Hypothyroidism

• Infarction (sickle cell anemia)

• Larsen syndrome

• Mucolipidosis II

• Mucopolysaccharidoses

• Multiple epiphyseal dysplasia

• Myotonic dystrophy (Steinert syndrome)

• Nevoid basal cell carcinoma syndrome (Gorlin syndrome)

• Osteoglophonic syndrome

• Otopalatodigital syndrome, type 2

• Pallister-Hall syndrome

• Poland syndrome

• Pseudohypoparathyroidism (Albright hereditary osteodystrophy)

• Pseudo-pseudohypoparathyroidism

• Refsum disease

• Rothmund-Thomson syndrome

• Ruvalcaba syndrome

• Short rib-polydactyly syndrome (types 1,2, and 3)

• Sickle cell anemia

• Silver-Russel syndrome

• Sjögren-Larsson syndrome

• Trauma (thermal, electrical, fracture)

• Tricho-rhino-phalangeal syndromes (types I, II, and III)

• Turner syndrome

• Weill-Marchesani syndrome

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