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2. Congenital ichthyosis, mental retardation, dwarfism and renal impairment: a new syndrome. Passwell JH; Goodman RM; Ziprkowski M; Cohen BE Clin Genet; 1975 Jul; 8(1):59-65. PubMed ID: 1149323 [TBL] [Abstract][Full Text] [Related]
3. The Tay syndrome (congenital ichthyosis with trichothiodystrophy). Happle R; Traupe H; Gröbe H; Bonsmann G Eur J Pediatr; 1984 Jan; 141(3):147-52. PubMed ID: 6538137 [TBL] [Abstract][Full Text] [Related]
4. [Rare syndrome: hereditary ataxia with congenital cataract and mental retardation]. FRANCESCHETTI A; KLEIN D; MARTY F Confin Neurol; 1956; 16(4-5):271-5. PubMed ID: 13384021 [No Abstract] [Full Text] [Related]
5. MENTAL RETARDATION: METHODS OF DIAGNOSIS AND SOME RECENTLY DESCRIBED SYNDROMES. RICHARDS BW Can Med Assoc J; 1963 Nov; 89(20):1024-9. PubMed ID: 14081787 [TBL] [Abstract][Full Text] [Related]
6. [Ichthyosis vulgaris, growth retardation, hair dysplasia, tooth abnormalities, immunologic deficiencies, psychomotor retardation and resorption disorders. Case report of 2 siblings]. Braun-Falco O; Ring J; Butenandt O; Selzle D; Landthaler M Hautarzt; 1981 Feb; 32(2):67-74. PubMed ID: 7228665 [TBL] [Abstract][Full Text] [Related]
7. Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities. A link between the ichthyosis-associated and BIDS syndromes. Jorizzo JL; Crounse RG; Wheeler CE J Am Acad Dermatol; 1980 Apr; 2(4):309-17. PubMed ID: 7364988 [TBL] [Abstract][Full Text] [Related]
8. [On the syndrome: ichthyosis congenita, feeblemindedness and spastic disorders of the type of Little's disease]. GREITHER A Hautarzt; 1959 Sep; 10():403-8. PubMed ID: 13851752 [No Abstract] [Full Text] [Related]
12. Two sisters with mental retardation, cataract, ataxia, progressive hearing loss, and polyneuropathy. Begeer JH; Scholte FA; van Essen AJ J Med Genet; 1991 Dec; 28(12):884-5. PubMed ID: 1661780 [TBL] [Abstract][Full Text] [Related]
13. [Ultrastructure of inborn erors of keratinization. I. Ichthyosis congenita]. Anton-Lamprecht I Arch Dermatol Forsch; 1972; 243(2):88-100. PubMed ID: 5052861 [No Abstract] [Full Text] [Related]
14. [A SPORADIC CASE OF MARINESCO-SJOGREN SYNDROME]. PERALTASERRANO A Acta Pediatr Esp; 1965 Apr; 23():315-30. PubMed ID: 14347509 [No Abstract] [Full Text] [Related]
15. [MARINESCO-SJOEGREN SYNDROME]. ABRAMOVICH GB; KHARITONOV RA Zh Nevropatol Psikhiatr Im S S Korsakova; 1964; 64():1028-34. PubMed ID: 14249758 [No Abstract] [Full Text] [Related]
16. An extremely rare recessive hereditary syndrome including cerebellar ataxia, oligophrenia, cataract, and other features. GARLAND H; MOORHOUSE D J Neurol Neurosurg Psychiatry; 1953 May; 16(2):110-6. PubMed ID: 13053231 [No Abstract] [Full Text] [Related]
17. Trichothiodystrophy-neurotrichocutaneous syndrome of Pollitt: a report of two unrelated cases. King MD; Gummer CL; Stephenson JB J Med Genet; 1984 Aug; 21(4):286-9. PubMed ID: 6492094 [TBL] [Abstract][Full Text] [Related]
18. The puppet-like syndrome of Angelman. Dooley JM; Berg JM; Pakula Z; MacGregor DL Am J Dis Child; 1981 Jul; 135(7):621-4. PubMed ID: 7246489 [TBL] [Abstract][Full Text] [Related]
19. The Rud syndrome: ichthyosis, hypogonadism, mental retardation. Nissley PS; Thomas GH Birth Defects Orig Artic Ser; 1971 Jun; 7(8):246-7. PubMed ID: 5173271 [No Abstract] [Full Text] [Related]
20. [OLIGOPHRENIA, ATAXIA, BILATERAL CATARACT (MARINESCO-SJOEGREN SYNDROME) ASSOCIATED WITH CONGENITAL TOXOPLASMOSIS]. ZLATOVEROV AI; IARTSEVA LV; KRSILNIKOVA NA Zh Nevropatol Psikhiatr Im S S Korsakova; 1963; 63():1478-81. PubMed ID: 14183977 [No Abstract] [Full Text] [Related] [Next] [New Search]