Facial hypoplasia

Hypoplasia (from Ancient Greek ὑπo- hypo-, "under" + πλάσις plasis, "formation"; adjective form hypoplastic) is underdevelopment or incomplete development of a tissue or organ. Although the term is not always used precisely, it properly refers to an inadequate or below-normal number of cells. [Source: Wikipedia ]

May Be Caused by
3-M syndrome
Aarskog syndrome
Acromesomelic dysplasia
Anderson syndrome
Antley-Bixler syndrome
Binder syndrome
Bloom syndrome
Branchiogenitoskeletal syndrome
Campomelic dysplasia
Chondrodysplasia punctata Conradi-Hünermann type
Chondrodysplasia punctata rhizomelic type
Chondrodysplasia punctata tibial-metacarpal type
Cleidocranial dysostosis
Cowden syndrome
Craniofrontonasal dysplasia
Crouzon syndrome
Distal arthrogryposis type 2A
Dyssegmental dysplasia
Familial hemifacial microsomia with radial limb defect
Femoral hypoplasia-unusual facies syndrome
Fetal alcohol syndrome
Fetal valproate syndrome
Frontofacionasal dysplasia
Frontonasal dysplasia
GAPO syndrome
Gerodermia osteodysplastica
Goldberg-Shprintzen syndrome
Goltz syndrome
Gorlin-Chaudhry-Moss syndrome
Hajdu-Cheney syndrome
Hallermann-Streiff syndrome
Keutel syndrome
Kniest dysplasia
Kyphomelic dysplasia
Larsen syndrome
Lethal osteosclerotic skeletal dysplasia Raine type
Mandibuloacral dysplasia
Mandibulofacial dysostosis and tibial hemimelia
Maxillofacial dysostosis
Mesomelic dysplasia
Microcephalic osteodysplastic dysplasia
Myhre syndrome
Nager acrofacial dysostosis
Nonerupting teeth-maxillozygomatic hypoplasia
Oculo-auriculo-vertebral spectrum
Oral-acral anomaly Verloes-Koulischer type
Osteoglophonic dysplasia
Otopalatodigital dysplasia type 2
Otospondylomegaepiphyseal dysplasia
Pierpont syndrome
Postaxial acrofacial dysostosis Miller type
Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema
Rieger syndrome
Schinzel-Giedion syndrome
Schneckenbecken dysplasia
Seckel syndrome
Spondyloepimetaphyseal dysplasia short limb-hand abnormal calcification type
Stickler syndrome
Tattoo dysplasia
Treacher Collins syndrome
Trichorhinophalangeal dysplasia
Trisomy 18
Trisomy 21
Tuomaala syndrome
Weill-Marchesani syndrome
Weissenbacher-Zweymüller phenotype
Wiedemann-Rautenstrauch syndrome
Wildervanck syndrome
Wrinkly skin syndrome
Yunis-Varon syndrome