نتایج جستجو برای: cutis marmorata telangictatica congenital

تعداد نتایج: 122724  

Journal: :Archives of disease in childhood 1993
J Verbov

Aplasia cutis and other scarring alopecias Congenital absence of skin (aplasia cutis) presents on the scalp as one or more noninflammatory well defined oval or circular ulcers, crusted areas (fig 1) or as scars. Lesions usually occur over the vertex in or adjacent to the midline and may involve skin only or occasionally may extend deeply to bone and dura. Complications include secondary infecti...

Journal: :world journal of plastic surgery 0
waleed alshehri department of plastic and reconstructive surgery, king fahd medical city, riyadh, saudi arabia sara alfadil department of plastic and reconstructive surgery, king fahd medical city, riyadh, saudi arabia alhanouf alothri department of plastic and reconstructive surgery, king fahd medical city, riyadh, saudi arabia abdulaziz o. alabdulkarim department of plastic and reconstructive surgery, king fahd medical city, riyadh, saudi arabia shabeer a. wani department of plastic and reconstructive surgery, king fahd medical city, riyadh, saudi arabia sari m. rabah department of plastic and reconstructive surgery, king fahd medical city, riyadh, saudi arabia

aplasia cutis conginita (acc) is a condition characterized by congenital absence of skin, usually on the scalp. acc can occur as an isolated condition or in the presence of other congenital anomalies. here we describe a case of a 16 days old baby girl with an isolated acc of the scalp. her elder two siblings have been diagnosed with acc with concomitant cardiac or limb anomalies. the patient wa...

Journal: :Indian pediatrics 1995
B C Bakane B Patil

Aplasia cutis congenita is a rare developmental anomaly that most commonly involves vertex of the scalp and may be associated with other congenital anomalies. Although isolated congenital absence of skin and congenital knee contracture is known,, association of these two conditions is not reported. We report on a child with absence of skin of left lower limb with contracture of left knee at birth.

Journal: :Oxford Medical Case Reports 2019

2012
Farrukh Mahmood Shahzadi Tasneem Malik Muhammad Nadeem

Aplasia cutis congenita is a rare congenital anomaly characterized by the absence of a patch of skin since birth. It may lead to life threatening complications at times. A 5-day-old neonate with Aplasia cutis congenita was received in a state of shock due to tremendous blood loss from the superior sagittal sinus. The neonate was resuscitated immediately followed by closure of the superior sagit...

2016
Shishira Bharadwaj Prakash Shrestha Tushar D. Gohel Maninder Singh

Cutis laxa (CL) is a rare connective tissue disorder characterized by phenotypic appearance of loose and redundant skin. CL can be congenital or acquired. Congenital forms include autosomal dominant, autosomal recessive and X-linked recessive. Apart from cutaneous abnormalities, CL can present with visceral involvement. In this article, we report a case of CL presenting as recurrent ileus.

2014
Majdouline Boujoual Fatima Jabouirik Jaouad Kouach Driss Moussaoui Mohammed Dehayni

Aplasia cutis congenital is a rare congenital absence of skin, exceptionally involves extremities. Most cases are sporadic but familial autosomal dominant pattern can be found. The etiology remains unclear, both genetic and environmental causes have been implicated. This lesion has primarily a clinical diagnosis. Imaging studies may be used to evaluate underlying tissues and investigate other c...

2017
Ariana Kariminejad Fariba Afroozan Bita Bozorgmehr Alireza Ghanadan Susan Akbaroghli Hamid Reza Khorram Khorshid Faezeh Mojahedi Aria Setoodeh Abigail Loh Yu Xuan Tan Nathalie Escande-Beillard Fransiska Malfait Bruno Reversade Thatjana Gardeitchik Eva Morava

Cutis laxa is a heterogeneous condition characterized by redundant, sagging, inelastic, and wrinkled skin. The inherited forms of this disease are rare and can have autosomal dominant, autosomal recessive, or X-linked inheritance. Three of the autosomal recessive cutis laxa syndromes, namely cutis laxa IIA (ARCL2A), cutis laxa IIB (ARCL2B), and geroderma osteodysplastica (GO), have very similar...

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