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2. Cataracts, alopecia, and sclerodactyly: a previously apparently undescribed ectodermal dysplasia syndrome on the island of Rodrigues. Wallis C; Ip FS; Beighton P Am J Med Genet; 1989 Apr; 32(4):500-3. PubMed ID: 2773993 [TBL] [Abstract][Full Text] [Related]
3. Hair loss in infancy. Moreno-Romero JA; Grimalt R G Ital Dermatol Venereol; 2014 Feb; 149(1):55-78. PubMed ID: 24566566 [TBL] [Abstract][Full Text] [Related]
4. Autosomal recessive inheritance of atrichia congenita. Cantú JM; Sánchez-Corona J; González-Mendoza A; Martínez y Martínez R; García-Cruz D Clin Genet; 1980; 17(3):209-12. PubMed ID: 7363508 [TBL] [Abstract][Full Text] [Related]
5. [Review of physiology and physiopathology of hair growth in children. II. Physiopathology of hair growth, alopecia areata and some genetically conditioned hair anomalies]. Bartosová L Cesk Dermatol; 1974 Dec; 49(6):367-74. PubMed ID: 4613486 [No Abstract] [Full Text] [Related]
6. Atrichias and hypotrichoses: a brief review with description of a recessive atrichia in two brothers. Pinheiro M; Freire-Maia N Hum Hered; 1985; 35(1):53-5. PubMed ID: 3972425 [No Abstract] [Full Text] [Related]
7. Phenotypic heterogeneity among the pilosebaceous dysplasias. Solomon LM Mod Probl Paediatr; 1975; 17():11-4. PubMed ID: 1186666 [No Abstract] [Full Text] [Related]
8. Pili torti and onychodysplasia. Report of a previously undescribed hidrotic ectodermal dysplasia. Calzavara-Pinton P; Carlino A; Benetti A; De Panfilis G Dermatologica; 1991; 182(3):184-7. PubMed ID: 1879585 [TBL] [Abstract][Full Text] [Related]
9. The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition. Hay RJ; Wells RS Br J Dermatol; 1976 Mar; 94(3):277-89. PubMed ID: 946410 [TBL] [Abstract][Full Text] [Related]
10. Autosomal recessive neurodegenerative disorder with trichorrhexis invaginata and ectodermal dysplasia. Gyure KA; Kurczynski TW; Gunning W; French BN Pediatr Neurol; 1992; 8(6):469-72. PubMed ID: 1476579 [TBL] [Abstract][Full Text] [Related]
11. Congenital atrichia, palmoplantar hyperkeratosis, mental retardation, and early loss of teeth in four siblings: a new syndrome? Steijlen PM; Neumann HA; der Kinderen DJ; Smeets DF; van der Kerkhof PC; Happle R J Am Acad Dermatol; 1994 May; 30(5 Pt 2):893-8. PubMed ID: 8169270 [TBL] [Abstract][Full Text] [Related]
12. Hair loss. Common congenital and acquired causes. Phillips JH; Smith SL; Storer JS Postgrad Med; 1986 Apr; 79(5):207-15. PubMed ID: 3960800 [TBL] [Abstract][Full Text] [Related]
13. Odontoonychodysplasia with alopecia: a new pure ectodermal dysplasia with probable autosomal recessive inheritance. Pinheiro M; Freire-Maia N; Gollop TR Am J Med Genet; 1985 Jan; 20(1):197-202. PubMed ID: 2982262 [TBL] [Abstract][Full Text] [Related]
14. Hair loss in children in South-East Nigeria: common and uncommon cases. Nnoruka EN; Obiagboso I; Maduechesi C Int J Dermatol; 2007 Oct; 46 Suppl 1():18-22. PubMed ID: 17919200 [TBL] [Abstract][Full Text] [Related]
16. Alopecia areata universalis in an infant. LaRow JA; Mysliborski J; Rappaport IP; Rouleau GA; Carlson JA J Cutan Med Surg; 2001; 5(2):131-4. PubMed ID: 11443485 [TBL] [Abstract][Full Text] [Related]
17. Aplasia cutis congenita, high myopia, and cone-rod dysfunction in two sibs: a new autosomal recessive disorder. Gershoni-Baruch R; Leibo R Am J Med Genet; 1996 Jan; 61(1):42-4. PubMed ID: 8741916 [TBL] [Abstract][Full Text] [Related]
19. A new type of pachyonychia congenita. van Steensel MA; Smith FJ; Steijlen PM Eur J Dermatol; 2001; 11(3):188-90. PubMed ID: 11358721 [TBL] [Abstract][Full Text] [Related]
20. The genetics of human hair growth. Porter PS Birth Defects Orig Artic Ser; 1971 Jun; 7(8):69-85. PubMed ID: 5173315 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]