From: A novel VPS13B mutation in Cohen syndrome: a case report and review of literature
Common | Less common |
---|---|
Craniofacial characteristics: | Musculoskeletal system: |
• Wave-shaped eyelids • Short philtrum • Thick hair • Low hairline • Long or thick eyelashes • Prominent root of nose • Thick eyebrow • Prominent upper central incisors • High or narrow plate • Microcephaly • Small or absent lobuli of ears | • Short stature • Mild syndactyly • Kyphoscoliosis • Cubitus valgum • Truncal obesity • Simian creases • Lumbar lordosis |
Ocular system: | |
• Downslanting palpebral fissures | |
Cardiovascular system: | |
Growth and Developmental abnormalities: | • Cardiac systolic murmur • Decreased left ventricular function in older patients • Floppy mitral valve and mitral regurgitation • Dilation in the descending aorta |
• Motor developmental delay • Speech delay • Non-progressive mental retardation • Delayed puberty • Low birth weight | |
Musculoskeletal system: | |
• Hypotonia • Hypermobile joints • Slender limbs • Pes planus • Wide gap between the first toe and the second toe • Genu valgum | Endocrine system: |
• Gonadotropin deficiency • Growth hormone deficiency • Insulin resistance • Non-insulin-dependent diabetes mellitus • Cryptorchidism | |
Nervous system: | |
• Motor clumsiness • Brisk reflexes • Cheerful disposition | |
Ocular system: | |
(Ophthalmic abnormalities are mostly seen in patients older than 5 years old and are progressive): • Retinochoroidal dystrophy • Myopia (mostly refractive type) | |
Gastrointestinal system: | |
• Neonatal feeding difficulties | |
Other: | |
• High-pitched voice • Reduced fetal activity |