Kenny Syndrome 6
General: Congenital syndrome.
Ocular: Nanophthalmos with hyperopia; papilledema; vascular tortuosity; macular crowding; bilateral optic atrophy.
Clinical: Dwarfism; thickened long bone cortex; transient hypocalcemia.
Boynton JR, et al. Ocular findings in Kenny's syndrome. Arch Ophthalmol 1979; 97:896-900.
Kenny FM, Linarelli L. Dwarfism and cortical thickening of tubular bones. Am J Dis Child 1966; 111:201-207.
Majewski F, et al. The Kenny syndrome: a rare type of growth deficiency with tubular stenosis, transient hypoparathyroidism and anomalies of refraction. Eur J Pediatr 1981; 136:21-30.
Rebolleda Fernandez G, et al. Bilateral optic atrophy in Kenny's syndrome. Acta Ophthalmol 1992; 70:135-l38.
Klippel- Trenaunay-Weber Syndrome (Parkes-Weber Syndrome; Angio-Osteo-Hypertrophy Syndrome) 6 General: Most frequently inherited as irregula [...] |
Simmonds Syndrome (Hypopituitarism Syndrome) General: Anterior pit [...] |
ML III (Pseudo-Hurler Polydystrophy; Mucolipidosis III) General: Autosomal [...] |
Copyright © 2010 - 2024
: eSanatos.com - Reproducerea, chiar si partiala, a materialelor de pe acest site este interzisa!
Informatiile medicale au scop informativ si educational. Ele nu pot inlocui consultul medicului si nici diagnosticul stabilit in urma investigatiilor si analizelor medicale la un medic specialist.
Termeni si conditii - Confidentialitatea datelor - Contact
Despre diseases |
| Alte sectiuni |
|
Ai o problema medicala? |
