Short metatarsal

Brachymetatarsia is a condition in which there is one or more abnormally short or overlapping toe bones (metatarsals). This condition may result due to a congenital defect or it may be an acquired condition. [Source: Wikipedia ]

May Cause
Congenital short hands and feet
Short first metacarpal
Short first metatarsal
May Be Caused by
Achondroplasia
Acrocephalosyndactyly Saethre-Chotzen type
Acrodysostosis
Acromesomelic dysplasia
Aplasia cutis congenita
Atelosteogenesis
Beckwith-Wiedemann syndrome
Biemond syndrome type 1
Brachmann-de Lange syndrome
Camptobrachydactyly
Cephaloskeletal dysplasia
CHILD syndrome
Chondrodysplasia punctata brachytelephalangic type
Chondrodysplasia punctata tibial-metacarpal type
Christian syndrome
Chromosome 18:del(18q) syndrome
Chromosome 5:del(5p) syndrome
Cockayne syndrome
Coffin-Siris syndrome
Cohen syndrome
Desbuquois dysplasia
Diastrophic dysplasia
Du Pan syndrome
Dyggve-Melchior-Clausen dysplasia
Dyschondrosteosis
Dyssegmental dysplasia
Enchondromatosis
Familial brachydactyly A1
Familial brachydactyly C
Familial brachydactyly E
Fanconi anemia
Fetal alcohol syndrome
Fibrodysplasia ossificans progressiva
Goltz syndrome
Gorlin syndrome
Grebe chondrodysplasia
Hand-foot-genital syndrome
Hereditary multiple exostoses
Holt-Oram syndrome
Hunter syndrome
Hurler syndrome
Hypochondroplasia
Hypoparathyroidism
Hypothyroidism
Ichthyosis syndrome
Infantile hypothyroidism
Juberg-Hayward syndrome
Larsen syndrome
Megaepiphyseal dwarfism
Metaphyseal chondrodysplasia McKusick type
Mucolipidosis type 2
Mucopolysaccharidosis
Multiple epiphyseal dysplasia
Myotonic dystrophy
Nager acrofacial dysostosis
Normal variant
Omodysplasia
Opitz trigonocephaly syndrome
Osteoglophonic dysplasia
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Pallister-Hall syndrome
Poland syndrome
Pseudodiastrophic dysplasia
Pseudohypoparathyroidism
Pseudopseudohypoparathyroidism
Radial ray syndrome
Refsum disease
Robinow syndrome
Rothmund-Thomson syndrome
Rubinstein-Taybi syndrome
Short rib-polydactyly syndrome
Silver-Russell syndrome
Sjögren-Larsson syndrome
Spondyloepimetaphyseal dysplasia
Spondyloperipheral dysplasia
Thanatophoric dysplasia
Trichorhinophalangeal dysplasia
Trisomy 18
Trisomy 9p
Turner syndrome
VATER association
Weill-Marchesani syndrome
Yunis-Varon syndrome
Achondroplasia
Acrocephalosyndactyly Saethre-Chotzen type
Acrodysostosis
Acromesomelic dysplasia
Aplasia cutis congenita
Atelosteogenesis
Beckwith-Wiedemann syndrome
Biemond syndrome type 1
Brachmann-de Lange syndrome
Camptobrachydactyly
Cephaloskeletal dysplasia
CHILD syndrome
Chondrodysplasia punctata brachytelephalangic type
Chondrodysplasia punctata tibial-metacarpal type
Christian syndrome
Chromosome 18:del(18q) syndrome
Chromosome 5:del(5p) syndrome
Cockayne syndrome
Coffin-Siris syndrome
Cohen syndrome
Desbuquois dysplasia
Diastrophic dysplasia
Du Pan syndrome
Dyggve-Melchior-Clausen dysplasia
Dyschondrosteosis
Dyssegmental dysplasia
Enchondromatosis
Familial brachydactyly A1
Familial brachydactyly C
Familial brachydactyly E
Fanconi anemia
Fetal alcohol syndrome
Fibrodysplasia ossificans progressiva
Goltz syndrome
Gorlin syndrome
Grebe chondrodysplasia
Hand-foot-genital syndrome
Hereditary multiple exostoses
Holt-Oram syndrome
Hunter syndrome
Hurler syndrome
Hypochondroplasia
Hypoparathyroidism
Hypothyroidism
Ichthyosis syndrome
Infantile hypothyroidism
Juberg-Hayward syndrome
Larsen syndrome
Megaepiphyseal dwarfism
Metaphyseal chondrodysplasia McKusick type
Mucolipidosis type 2
Mucopolysaccharidosis
Multiple epiphyseal dysplasia
Myotonic dystrophy
Nager acrofacial dysostosis
Normal variant
Omodysplasia
Opitz trigonocephaly syndrome
Osteoglophonic dysplasia
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Pallister-Hall syndrome
Poland syndrome
Pseudodiastrophic dysplasia
Pseudohypoparathyroidism
Pseudopseudohypoparathyroidism
Radial ray syndrome
Refsum disease
Robinow syndrome
Rothmund-Thomson syndrome
Rubinstein-Taybi syndrome
Short rib-polydactyly syndrome
Silver-Russell syndrome
Sjögren-Larsson syndrome
Spondyloepimetaphyseal dysplasia
Spondyloperipheral dysplasia
Thanatophoric dysplasia
Trichorhinophalangeal dysplasia
Trisomy 18
Trisomy 9p
Turner syndrome
VATER association
Weill-Marchesani syndrome
Yunis-Varon syndrome