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Handchirurgie · Mikrochirurgie · Plastische Chirurgie, 2016
Aplasia cutis congenita is a rare congenital disorder characterised by the absence of skin. It mostly affects the scalp, but may also involve deeper tissue layers such as bone or dura mater. Bleeding from the sagittal sinus and infections are the most common complications.
J, Steinbacher, T, Rath, C-H J, Tzou
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Aplasia cutis congenita is a rare congenital disorder characterised by the absence of skin. It mostly affects the scalp, but may also involve deeper tissue layers such as bone or dura mater. Bleeding from the sagittal sinus and infections are the most common complications.
J, Steinbacher, T, Rath, C-H J, Tzou
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Oral and Maxillofacial Surgery, 2010
A case of unilateral aplasia is reported. Associated anatomical anomalies and review of the literature is described, and a comparison with maxillary sinus hypoplasia is made.A 40-year-old male was complaining of an esthetic "defect" in his face. There was an antero-posterior depression in the left infraorbital region. Computed tomography showed absence
Bruno Ramos, Chrcanovic +1 more
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A case of unilateral aplasia is reported. Associated anatomical anomalies and review of the literature is described, and a comparison with maxillary sinus hypoplasia is made.A 40-year-old male was complaining of an esthetic "defect" in his face. There was an antero-posterior depression in the left infraorbital region. Computed tomography showed absence
Bruno Ramos, Chrcanovic +1 more
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Archives of Ophthalmology, 1992
Optic nerve aplasia is a rare congenital defect invariably associated with other ocular or systemic disorders. We examined a 3-year-old girl with monocular microphthalmos who had optic nerve aplasia on histopathologic examination of the eye after enucleation.
C E, Margo +3 more
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Optic nerve aplasia is a rare congenital defect invariably associated with other ocular or systemic disorders. We examined a 3-year-old girl with monocular microphthalmos who had optic nerve aplasia on histopathologic examination of the eye after enucleation.
C E, Margo +3 more
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Radiology, 1960
Congenital absence of part or all of the sacrum is of infrequent occurrence. Gross aplasia (frequently called agenesis) of the caudal portion of the spine from the mid-thoracic level or higher is probably incompatible with life at an early stage of fetal development and would therefore tend to be unreported.
M J, GRAND, S, EICHENFELD, H G, JACOBSON
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Congenital absence of part or all of the sacrum is of infrequent occurrence. Gross aplasia (frequently called agenesis) of the caudal portion of the spine from the mid-thoracic level or higher is probably incompatible with life at an early stage of fetal development and would therefore tend to be unreported.
M J, GRAND, S, EICHENFELD, H G, JACOBSON
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Plastic and Reconstructive Surgery, 1980
Aplasia cutis congenita is an uncommon condition; fewer than 300 cases have been reported in the literature. Usually, the condition occurs as a focal scalp ulcer, but it may involve the full thickness of the skull or other areas of the body. Most lesions require coverage with a scalp flap, though only observation or split-thickness skin grafts may be ...
G B, Irons, R M, Olson
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Aplasia cutis congenita is an uncommon condition; fewer than 300 cases have been reported in the literature. Usually, the condition occurs as a focal scalp ulcer, but it may involve the full thickness of the skull or other areas of the body. Most lesions require coverage with a scalp flap, though only observation or split-thickness skin grafts may be ...
G B, Irons, R M, Olson
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The Indian Journal of Pediatrics, 2000
Two cases of aplasia cutis congenita are reported here. One of the cases also had pre- and postaxial polydactyly and other digital anomalies.
A, Kumar, B B, Agrawal, B D, Bhatia
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Two cases of aplasia cutis congenita are reported here. One of the cases also had pre- and postaxial polydactyly and other digital anomalies.
A, Kumar, B B, Agrawal, B D, Bhatia
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Neuropediatrics, 1996
We describe three children with unilateral cerebellar aplasia (UCA). Deliveries at term and neonatal periods were uneventful. Pregnancy was normal in one and complicated by mild bleeding (in second and fourth month respectively) in two instances. Presenting signs were delayed motor development with marked contralateral torticollis (n = 1), hemiplegia ...
E, Boltshauser +3 more
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We describe three children with unilateral cerebellar aplasia (UCA). Deliveries at term and neonatal periods were uneventful. Pregnancy was normal in one and complicated by mild bleeding (in second and fourth month respectively) in two instances. Presenting signs were delayed motor development with marked contralateral torticollis (n = 1), hemiplegia ...
E, Boltshauser +3 more
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Journal of the American Academy of Dermatology, 1985
We report a family with aplasia cutis congenita, an extremely rare condition. Particular attention is paid to the clinical, etiologic, and genetic characteristics. The only possible treatment, as in the first case in this family, is excision and reconstruction by dermatologic surgery procedures.
P, Sánchez-Pedreño Guillén +2 more
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We report a family with aplasia cutis congenita, an extremely rare condition. Particular attention is paid to the clinical, etiologic, and genetic characteristics. The only possible treatment, as in the first case in this family, is excision and reconstruction by dermatologic surgery procedures.
P, Sánchez-Pedreño Guillén +2 more
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Archives of Pediatrics & Adolescent Medicine, 1954
CONGENITAL aplasia of the adrenal glands has been noted previously to occur in cases of cranial anomaly, such as an encephalus or hydrocephalus, or other central-nervous-system malformations extensive enough to involve the pituitary gland. There have been cases of Addison's disease in adults in which at autopsy the adrenals could not be found.
J B, WELSH, G B, MEHLIN
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CONGENITAL aplasia of the adrenal glands has been noted previously to occur in cases of cranial anomaly, such as an encephalus or hydrocephalus, or other central-nervous-system malformations extensive enough to involve the pituitary gland. There have been cases of Addison's disease in adults in which at autopsy the adrenals could not be found.
J B, WELSH, G B, MEHLIN
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Archives of Dermatology, 1962
Congenital defect of the skin constitutes one of the rare and interesting anomalies peculiar to the newborn. Its extreme rarity, in comparison with the great frequency of minor aberrations such as disturbances of pigment, hair, glandular development, and vascular supply, can only mean that the natural, inherent factors at work in covering the body with
R R, RAUSCHKOLB, S I, ENRIQUEZ
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Congenital defect of the skin constitutes one of the rare and interesting anomalies peculiar to the newborn. Its extreme rarity, in comparison with the great frequency of minor aberrations such as disturbances of pigment, hair, glandular development, and vascular supply, can only mean that the natural, inherent factors at work in covering the body with
R R, RAUSCHKOLB, S I, ENRIQUEZ
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