Seckel syndroom
| Seckel syndroom | Seckel syndrome , or microcephalic primordial dwarfism also known as bird-headed dwarfism , Harper's syndrome , Virchow—Seckel dwarfism and bird-headed dwarf of Seckel [ 1 ] is an extremely rare congenital nanosomic disorder. |
| Seckel syndrome (SCKL) | A rare form of microcephalic primordial dwarfism characterized by a proportionate dwarfism of prenatal onset, a severe microcephaly, a typical dysmorphic face bird-like , and mild to severe intellectual disability. |
| Seckel | Seckel syndrome is a rare inherited syndrome, named for the pediatrician, Dr. |
| Seckel syndrome - Wikipedia | . |
Seckel syndroom
- FDNA™Seckel Syndrome: Symptoms, Causes and Diagnosis Seckel Syndrome, sometimes referred to as 'bird-headed dwarfism', is an autosomal recessive disorder. It primarily affects physical development, leading to distinctive dysmorphic features .
- Orphanet: Seckel syndrome Seckel syndrome is a genetic disorder characterized by growth retardation, very small head (microcephaly(with intellectual disability, and unique facial features such as large eyes, beak .
- O síndrome de Seckel, uma patologia autossómica recessiva, é a forma mais comum de nanismo osteodisplásico microcefálico. Caracteriza-se por nanismo proporcionado de aparecimento .
- What is Seckel syndrome? Seckel syndrome is characterized by a proportionate dwarfism of prenatal onset, a severe microcephaly with a bird-headed like appearance and mental retardation. Hematological .