Narrow face

Narrow face is seen in the following conditions and syndromes: • 5p partial monosomy syndrome • Bloom syndrome • Branchiootorenal syndrome 1 • Cardiofaciocutaneous syndrome 4 • Christianson syndrome • Congenital disorder of glycosylation, type IIw • Congenital myasthenic syndrome 2A • Congenital myopathy 4A, autosomal dominant • Congenital myopathy 4B, autosomal recessive • Creatine transporter deficiency • Cutis laxa, X-linked • Ehlers-Danlos syndrome, Beasley-Cohen type • Granulocytopenia with immunoglobulin abnormality • Hereditary spastic paraplegia 23 and 51 • Intellectual disability, autosomal recessive 5 • Intellectual disability, X-linked 107, 58, and 61 • Knobloch syndrome • Marfan syndrome • Mitochondrial DNA depletion syndrome 13 • Nance-Horan syndrome • Oculofaciocardiodental syndrome • Otofaciocervical syndrome 1 • Proximal myopathy with extrapyramidal signs • Radioulnar synostosis-developmental delay-hypotonia syndrome • Renpenning syndrome • Seckel syndrome 9 • Severe X-linked myotubular myopathy • SIN3A-related intellectual disability syndrome due to a point mutation • Symphalangism-brachydactyly syndrome • Syndromic X-linked intellectual disability 14 • Torsion dystonia 4 • X-linked intellectual disability with marfanoid habitus • XFE progeroid syndrome == See also ==