Hallermann-Streiff-Francois- syndrome. (Oculo-mandibulo-dyscrania with hypotrichosis) . a most characteristic syndrome with dyscrania and hypotrichosis, facial and eye anomalies and dwarfism
Wiedemann, H.R.; Dibbern, H.
Die Medizinische Welt 31(4): 134-135
1980
ISSN/ISBN: 0025-8512 PMID: 6767893 Document Number: 163859
Document emailed within 1 workday
Related Documents
Stolovitch, H.; Bracha, R.; Godel, V. 1984: Oculo-mandibulo-facial syndrome Harefuah 107(11): 330-332Rudobielski, R.; Rudzińska, A. 1972: Case of Hallermann-Streiff syndrome Klinika Oczna 42(4): 1087-1089
Gerinec, A.; Spissáková, B.; Chynoranský, M. 1989: The Hallermann-Streiff syndrome in 2 generations Ceskoslovenska Oftalmologie 45(5): 326-333
Aynaci, F.M.; Ozdemir, M.; Işik, Y. 1997: Atrial septal defect in Hallermann Streiff syndrome Genetic Counseling 8(2): 145-146
Sohi, B.K.; Boparai, M.S.; Sohi, A.S. 1978: Mandibulo oculo facial dyscephaly: a case report Indian Pediatrics 15(6): 521-522
Salamon, T.; Sućur, D.; Nikulin, A.; Lazović-Tepavac, O.; Topić, B.; Huml, I.; Dojcinov, D. 1991: Palmoplantar epidermal atrophy with hypokeratosis, dys- and hypotrichosis, hypodontia, enamel and dentin hypoplasia, isolated cleft palate with cleft uvula, strabismus cryptorchism and other anomalies--an undescribed ecto-mesodermal dysplasia? Der Hautarzt; Zeitschrift für Dermatologie Venerologie und verwandte Gebiete 42(4): 237-241
Krauze, M.; Waclawczyk, H.; Marek, J.; Swiszcz, A.; Stoińska, H. 1973: Syndrome of congenital facial and finger anomalies associated with mental deficiency in an infant (Rubinstein-Taybi syndrome) Polski Tygodnik Lekarski 28(49): 1947-1949
Kapoor, S.; Kapur, N. 2004: Branchio-oculo-facial syndrome with valvular pulmonic stenosis Indian Pediatrics 41(11): 1180-1181
Khalilov, I.M.; Avanesov, A.A.; Ganiev, K.D. 1977: Congenital alopecia and hypotrichosis Vestnik Dermatologii i Venerologii 8: 66-68
Prigent, F. 1999: Neonatal alopecia and hypotrichosis Annales de Dermatologie et de Venereologie 126(12): 975-980
Battin, J. 1974: Oculo-facial paralysis with osseous abnormalities and nanism: a particular aspect of the Moebius syndrome Journal de Genetique Humaine 22(3): 199-204
Schweiger, E.S.; Pinchover, L.; Bernstein, R.M. 2012: Topical bimatoprost for the treatment of eyebrow hypotrichosis Journal of Drugs in Dermatology: Jdd 11(1): 106-108
Ibsen, H.H.; Clemmensen, O.J.; Brandrup, F. 1991: Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations Acta Dermato-Venereologica 71(4): 349-351
Vantrappen, G.; Feenstra, L.; Fryns, J.P. 2000: Conductive hearing loss and multiple pre- and supra-auricular skin defects: a variant example of the Branchio-Oculo-Facial syndrome Genetic Counseling 11(3): 273-276
Koch, H.J.; Hübner, U.; Schaarschmidt, E.; Thiel, W. 1991: Keratosis palmoplantaris with clubbed fingers, hypotrichosis, hypohidrosis and dental dysplasia Der Hautarzt; Zeitschrift für Dermatologie Venerologie und verwandte Gebiete 42(6): 399-401
Purcaro, A.; Caruso, L.; Ciampani, N.; Inglese, L. 1976: Horseshoe lung, cardiac malposition and pulmonary vascular anomalies: a characteristic syndrome Giornale Italiano di Cardiologia 6(2): 312-316
Aarskog, D. 1971: A familial syndrome of short stature associated with facial dysplasia and genital anomalies Birth Defects Original Article Series 7(6): 235-239
Matthews-Brzozowska, T.; Baranowska, J.; Rogiński, P.; Obersztyn, E.; Cudziło, D. 2015: Malocclusions and craniofacial anomalies in a child with velo-cardio-facial syndrome Developmental Period Medicine 19(4): 490-495
Bork, K.; Stender, E.; Schmidt, D.; Berzas, C.; Rochels, R. 1987: Familial congenital hypotrichosis with "uncombable hair," retinal pigmentary dystrophy, juvenile cataract and brachymetacarpia: another entity of the ectodermal dysplasia group Der Hautarzt; Zeitschrift für Dermatologie Venerologie und verwandte Gebiete 38(6): 342-347
Reich, H. 1980: Meyer-Schwickerath-Weyers syndrome (oculo-dento-digital syndrome) Der Hautarzt; Zeitschrift für Dermatologie Venerologie und verwandte Gebiete 31(9): 515