References
- Souied E, Amalric P, Chauvet M-L, Chevallier C, Le Hoang P, Munnich A, Kaplan J. Unusual association of juvenile macular dystrophy with congenital hypotrichosis: occurrence in two siblings suggesting autosomal recessive inheritance. Ophthalmic Genet 1995; 16: 11–15
- Winter R M, Baraitser M. Multiple Congenital Anomalies. Chapman and Hall Medical, London 1991; 22–23; 185
- Albrectsen B, Svendsen I B. Hypotrichosis, syndactyly, and retinal degeneration in two siblings. Acta Dermato-Venerol 1956; 36: 96–101
- Ohdo S, Hirayama K, Terawaki T. Association of ectodermal dysplasia, ectrodactyly, and macular dystrophy: the eem syndrome. J Med Genet 1983; 20: 52–57
- Küster W, Majewski F, Hammerstein W. Alopecia, macular degeneration, and growth retardation: a new syndrome. Am J Med Genet 1987; 28: 477–481
- Marren P, Wilson C, Dawber R PR, Walshe M M. Hereditary hypotrichosis (Marie-Unna type) and juvenile macular degeneration (Stargardt's maculopathy). Clin Exp Dermatol 1992; 17: 189–191
- Albrectsen B, Svendsen I B. Hypotrichosis, syndactyly, and retinal degeneration in two siblings. Acta Dermato-Venerol 1956; 36: 96–101
- Marren P, Wilson C, Dawber R PR, Walshe M M. Hereditary hypotrichosis (Marie-Unna type) and juvenile macular degeneration (Stargardt's maculopathy). Clin Exp Dermatol 1992; 17: 189–191