Phenotypes for disease #05595 (CS (Cockayne syndrome (CS)))

9 entries on 1 page. Showing entries 1 - 9.
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0000173469 Cockayne syndrome CSA - - - - - - SIB - Livia Famiglietti 00230985
0000173470 Cockayne syndrome CSA - - - - - - SIB - Livia Famiglietti 00230986
0000173471 Cockayne syndrome CSA - - - - - - SIB - Livia Famiglietti 00230987
0000173472 Cockayne syndrome CSA - - - - - - SIB - Livia Famiglietti 00230988
0000173473 Cockayne syndrome CSA - - - - - - SIB - Livia Famiglietti 00230989
0000173474 Cockayne syndrome CSA - - - - - - SIB - Livia Famiglietti 00230990
0000231958 Cockayne syndrome type II - uneventful antenatal period;4-6m microcephaly, micrognathia, contractures knees and elbows, hypertonic, dislocated radial head, deep-set eyes, skeletal abnormalities, camptodactyly, adducted thumbs, stiff limbs, steeply sloping acetabulae, wrist contracture, slender long bones with mildly flared metaphyses, moderate kyphoscoliosis; brisk reflexes, no feeding problems; MRI brain at birth possible polymicrogyria; NMR 4m-large bilateral subdurals (>2 cm in depth), no major visible malformations; ECG 9m-abnormal; 16m-nystagmus, no other ophthalmic abnormalities, corneas completely clear, no cataracts; 2.5y-deceased Familial, autosomal recessive 02y06m - - - Johan den Dunnen 00306117
0000231962 Cockayne syndrome - prenatal microcephaly; born 41w, weight 2.9 kg, OFC 9th percentile first few months, OFC 1y-<2nd percentile; first year developed normally; 5y-multiple unusual plantar warts hands and forearms, unusual freckling hands and back of neck, tended to burn easily and quickly, no bad blisterering when exposed to sunlight; 7y-deep-set eyes, progressive scoliosis, multiple contractures feet, required lengthening Achilles tendon because of muscle cramps in hamstrings and calves; skin deeply pigmented, rashes, flat freckles; moderate bilateral hearing impairment, especially higher tones (<3y-normal hearing), short stature (height 110.4 cm [<2nd percentile], weight of 16.3 kg [<3rd percentile]), microcephaly (OFC 45.5 cm [<2nd percentile]), circulatory problems, bilateral astigmatism, no cataracts, attention deficit hyperactivity disorder, learning disability; MRI brain 3y-some delayed myelination, 7y-basal ganglia T1 shortening; severe migraines and headaches, ambulation lessened over time, gastrostomy-jejunostomy tube for feeding Familial, autosomal recessive 16y - - - Johan den Dunnen 00306119
0000231965 Cockayne syndrome - see paper; ..., 12y-deceased Familial, autosomal recessive 12y - - - Johan den Dunnen 00306122
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