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Items: 1 to 20 of 41

1.

Acromegaloid facial appearance and hypertrichosis: a case suggesting autosomal recessive inheritance.

Zen PR, Schwartz IV, Paskulin GA.

Clin Dysmorphol. 2004 Jan;13(1):49-50.

PMID:
15127769
2.

Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly).

Lazalde B, Sánchez-Urbina R, Nuño-Arana I, Bitar WE, de Lourdes Ramírez-Dueñas M.

Am J Med Genet. 2000 Oct 23;94(5):421-7. Review.

PMID:
11050630
3.

Hypertrichosis cubiti: two new cases and a review of the literature.

Visser R, Beemer FA, Veenhoven RH, De Nef JJ.

Genet Couns. 2002;13(4):397-403. Review.

PMID:
12558109
4.

[Tooth and oral mucosa hereditary anomalies in complex syndromes characterized by hyper- or hypotrichosis].

Giannetti L, Consolo U, Bambini F.

Minerva Stomatol. 2003 Jan-Feb;52(1-2):25-30. Review. Italian.

PMID:
12686911
5.

Hypertrichosis cubiti (hairy elbow syndrome): a clue to a malformation syndrome.

Polizzi A, Pavone P, Ciancio E, La Rosa C, Sorge G, Ruggieri M.

J Pediatr Endocrinol Metab. 2005 Oct;18(10):1019-25. Review.

PMID:
16355816
6.

Congenital vocal cord paralysis with possible autosomal recessive inheritance: case report and review of the literature.

Koppel R, Friedman S, Fallet S.

Am J Med Genet. 1996 Aug 23;64(3):485-7. Review.

PMID:
8862626
7.

Hypertrichosis terminalis, gingival hyperplasia, and a characteristic face: a new distinct entity.

Canún S, Guevara-Sanginés EG, Elvira-Morales A, Sierra-Romero Mdel C, Rodríguez-Asbun H.

Am J Med Genet A. 2003 Jan 30;116A(3):278-83. Review.

PMID:
12503107
8.

Microcephaly-lymphoedema-chorioretinal dysplasia: three cases to delineate the facial phenotype and review of the literature.

Vasudevan PC, Garcia-Minaur S, Botella MP, Perez-Aytes A, Shannon NL, Quarrell OW.

Clin Dysmorphol. 2005 Jul;14(3):109-16. Review.

PMID:
15930898
9.

Mental retardation in a boy with anterior cervical hypertrichosis.

Corona-Rivera JR, González-Abarca S, Hernández-Rocha J, García-Cruz D, Corona-Rivera A.

Am J Med Genet A. 2005 May 15;135(1):69-71. Review.

PMID:
15800907
10.

[Baller-Gerold syndrome].

Satokata I.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):136-7. Review. Japanese. No abstract available.

PMID:
11057169
11.

[Robinow syndrome].

Kawame H.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):236-7. Review. Japanese. No abstract available.

PMID:
11057211
12.

Oculodentodigital dysplasia: study of ophthalmological and clinical manifestations in three boys with probably autosomal recessive inheritance.

Frasson M, Calixto N, Cronemberger S, de Aguiar RA, Leão LL, de Aguiar MJ.

Ophthalmic Genet. 2004 Sep;25(3):227-36. Review.

PMID:
15512999
13.

Three patients with the osteochondrodysplasia and hypertrichosis syndrome--Cantu syndrome.

Rosser EM, Kaariainen H, Hurst JA, Baraitser M, Hall CM, Clayton P, Leonard JV.

Clin Dysmorphol. 1998 Apr;7(2):79-85. Review.

PMID:
9571276
14.

Gingival overgrowth, congenital generalized hypertrichosis, mental retardation and epilepsy: case report and overview.

Douzgou S, Mingarelli R, Dallapiccola B.

Clin Dysmorphol. 2009 Oct;18(4):205-8. doi: 10.1097/MCD.0b013e32832dc393. Review.

PMID:
19625955
15.

The syndrome of hypoparathyroidism, severe growth failure, developmental delay and distinctive facies.

al-Gazali LI, Dawodu A.

Clin Dysmorphol. 1997 Jul;6(3):233-7. Review.

PMID:
9220193
16.

[Acromegaloid facial appearance syndrome].

Matsuo M.

Ryoikibetsu Shokogun Shirizu. 2001;(33):134. Review. Japanese. No abstract available.

PMID:
11462367
17.

Oral-facial-skeletal syndromes.

Neri G, Gurrieri F, Genuardi M.

Am J Med Genet. 1995 Nov 20;59(3):365-8. Review. No abstract available.

PMID:
8599363
18.

[Isolated anterior cervical hypertrichosis].

Monteagudo B, Cabanillas M, de las Heras C, Cacharrón JM.

Actas Dermosifiliogr. 2009 Jan-Feb;100(1):61-4. Review. Spanish.

PMID:
19268113
19.

Oculoauriculovertebral spectrum: report of nine familial cases with evidence of autosomal dominant inheritance and review of the literature.

Vendramini-Pittoli S, Kokitsu-Nakata NM.

Clin Dysmorphol. 2009 Apr;18(2):67-77. doi: 10.1097/MCD.0b013e328323a7dd. Review.

PMID:
19305190
20.

Ambras syndrome: delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion (8) (p11.2; q22)

Baumeister FA, Egger J, Schildhauer MT, Stengel-Rutkowski S.

Clin Genet. 1993 Sep;44(3):121-8. Review.

PMID:
8275569

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