S Hadj-Rabia, A Rimella, A Smahi, S Fraitag… - Journal of the American …, 2011 - Elsevier Incontinentia pigmenti (IP) is a multisystem disorder, in which cutaneous symptoms can be accompanied by dental, ocular, and central nervous system defects. In adults, the clinical diagnosis of IP is based principally on the late onset of stage 4 lesions and their association with dental, ... Cited by 1 - Related articles - All 6 versions
DT Hsieh… - Archives of Neurology, 2011 - Am Med Assoc After an uncomplicated delivery, a newborn girl was found to have a rash consisting of semilinear rows of vesicles and hyperpigmented papules (Figure 1). The patient's neurological examination was otherwise unremarkable. Examination of the mother revealed faint hypopigmentation ...
M O'Doherty, K Mc Creery, AJ Green… - British Journal of …, 2011 - bjo.bmj.com Aim The aims of this study were to make an inventory of the disease in Ireland, to acquire better knowledge of the relationship between genetic makeup and phenotypic ocular presentation and, finally, through literature review and personal experience, to establish clear ... Cited by 2 - Related articles - All 4 versions
[HTML] from nih.govG Sanghi, MR Dogra, M Ray… - Indian Journal of …, 2011 - ncbi.nlm.nih.gov Incontinentia pigmenti (IP) (Bloch-Sulzberger syndrome) is an X-linked condition with dermatological, dental, neurological and ocular abnormalities. Ocular abnormalities occur in 25–77% cases of IP.[1] The characteristic manifestation is a proliferative retinopathy ... Related articles - All 4 versions
[HTML] from nih.govS Thakur, RD Puri, S Kohli, R Saxena… - The Indian Journal of …, 2011 - ncbi.nlm.nih.gov Incontinentia pigmenti (IP; Bloch- Sulzberger syndrome; MIM 308300) is a rare genodermatosis that occurs in approximately 1 in 50,000 newborns 1 – 4 . It is an X- linked dominant disorder that affects females and is lethal in utero for males. It is a multi- system disorder primarily ... Related articles - All 5 versions