Results 131 to 140 of about 8,789 (185)
Classification and developmental biology of congenital anomalies of the hand and upper extremity [PDF]
, 2009 Manske, Paul R., Oberg, Kerby C.
core +2 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2004
AbstractEctodermal dysplasias are a large group of heritable conditions characterized by congenital defects of one or more ectodermal structures and their appendages: hair (hypotrichosis, partial, or total alopecia), nails (dystrophic, hypertrophic, abnormally keratinized), teeth (enamel defect or absent), and sweat glands (hypoplastic or aplastic ...
Peter H, Itin, Susanna K, Fistarol
openaire +2 more sources
AbstractEctodermal dysplasias are a large group of heritable conditions characterized by congenital defects of one or more ectodermal structures and their appendages: hair (hypotrichosis, partial, or total alopecia), nails (dystrophic, hypertrophic, abnormally keratinized), teeth (enamel defect or absent), and sweat glands (hypoplastic or aplastic ...
Peter H, Itin, Susanna K, Fistarol
openaire +2 more sources
Dermatologic Clinics, 1987
In order to be considered an ectodermal dysplasia, a disorder should meet the following criteria: it must be congenital; it must be diffuse (not localized) and must involve the epidermis as well as at least one of its appendages; and it must not be progressive.
L M, Solomon, B, Cook, W, Klipfel
openaire +2 more sources
In order to be considered an ectodermal dysplasia, a disorder should meet the following criteria: it must be congenital; it must be diffuse (not localized) and must involve the epidermis as well as at least one of its appendages; and it must not be progressive.
L M, Solomon, B, Cook, W, Klipfel
openaire +2 more sources
Anhidrotic ectodermal dysplasia
The Indian Journal of Pediatrics, 1968Two typical cases of anhidrotic ectodermal dysplasia occurring in heterosexual siblings of a family are reported. The role of consanguinity in the parents regarding the severity of the defect in these two siblings is stressed.
A, Bhogaonkar, S K, Khanna
openaire +2 more sources
Dermatologica, 2009
Description of a patient presenting an hidrotic ectodermal dysplasia. Clinical signs were hypotrichosis, dystrophic nails, palmoplantar keratoderma, absence of teeth and hyperhidrosis.
G E, Pierard, D, Van Neste, B, Letot
openaire +2 more sources
Description of a patient presenting an hidrotic ectodermal dysplasia. Clinical signs were hypotrichosis, dystrophic nails, palmoplantar keratoderma, absence of teeth and hyperhidrosis.
G E, Pierard, D, Van Neste, B, Letot
openaire +2 more sources
Arthrogryposis and Ectodermal Dysplasia
Human Heredity, 1982Arthrogryposis, an unusual type of ectodermal dysplasia, growth retardation of prenatal onset, and diabetes mellitus were all present in the proposita and are unlikely to have arisen all independently. The combination of at least some of these abnormalities may represent a distinct syndrome.
G B, Côté +2 more
openaire +2 more sources
Acta Paediatrica, 1952
SummaryTwo case reports of ectodernial dysplasia in two females are presented. One case is believed to be the first reported with evidence of direct descent from mother to daughter. The other is a case of the mendelian dominant type. The submission is made that the anhydrotic type is not necessarily always a sex‐linked recessive manifestation in males ...
openaire +2 more sources
SummaryTwo case reports of ectodernial dysplasia in two females are presented. One case is believed to be the first reported with evidence of direct descent from mother to daughter. The other is a case of the mendelian dominant type. The submission is made that the anhydrotic type is not necessarily always a sex‐linked recessive manifestation in males ...
openaire +2 more sources
Anhidrotic Ectodermal Dysplasia
Plastic and Reconstructive Surgery, 1980A diagnosis of anhidrotic ectodermal dysplasia should be considered for patients with an undeveloped breast or other deformities. Recognition of the syndrome can lead to necessary and helpful genetic counseling and will ensure that other members of the family, who may also be affected by the syndrome, are under proper care.
R A, Ersek, H, Labandter, L, King
openaire +2 more sources