Search Results - Hind Alshihry, MD

Integrin α3 mutation junctional epidermolysis bullosa presenting with hypotrichosis and lacrimal obstruction by Hind Alshihry, MD, Shahad D. AlGhamdy, MD, Amal Alhashem, MD, Hind M. Almohanna, MD

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Vitamin B12 deficiency secondary to cobalamin F deficiency simulating dyskeratosis congenita by Lama Altawil, MD, Hind Alshihry, MD, Hala Ahmed, MD, Hanan E. Shamseldin, MD, Fowzan Alkuraya, MD

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Progressive symmetrical erythrokeratoderma manifesting as harlequin-like ichthyosis with severe thrombocytopenia secondary to a homozygous 3-ketodihydrosphingosine reductase mutati... by Lama Altawil, MD, Hind Alshihry, MD, Huda Alfaraidi, MD, Amal Alhashem, MD, Ahmed Alhumidi, MD, Fowzan S. Alkuraya, MD

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