face deformities

swollen feet, swollen feet and legs, swollen legs, weakness

Hypothyroidism is the disease state in humans and animals caused by insufficient production of thyroid hormone by the thyroid gland. There are several distinct causes for chronic hypothyroidism in human beings, the most common being Hashimoto's thyroiditis (an autoimmune disease) and radioiodine therapy for hyperthyroidism. Historically, iodine deficiency was the most common cause of hypothyroidism world-wide. The disease may also be caused by a lack of thyroid gland or a deficiency of hormones from either the hypothalamus or the pituitary. ... 

mouth breathing, nasal discharge, sinus congestion, stuffy nose

Nasal polyps are polypoidal masses arising mainly from the mucous membranes of the nose and paranasal sinuses. Nasal polyps are usually classified into antrochoanal polyps and ethmoidal polyps. Antrochoanal polyps arise from the maxillary sinuses and are much less common, ethmoidal polyps arise from the ethmoidal sinuses. Antrochoanal polyps are usually single and unilateral whereas ethmoidal polyps are multiple and bilateral. Symptoms of polyps include nasal block, sinusitis, anosmia or loss of smell, and secondary infection leading to headache. ... 

delayed development, learning problems, not gaining weight, restlessness

Fetal alcohol syndrome or FAS is a disorder of permanent birth defects that occurs in the offspring of women who drink alcohol during pregnancy. It is unknown whether amount, frequency or timing of alcohol consumption during pregnancy causes a difference in amount of damage done to the fetus. Thus, the current recommendation is not to drink at all during pregnancy. Alcohol crosses the placental barrier and can stunt fetal growth or weight, create distinctive facial stigmata, damage neurons and brain structures, and cause other physical, mental, or behavioral problems. ... 

blister(s) or bump(s) on face, diarrhea, palpitations, passing out

headache, increased sweating, urinating often, vomiting

Pituitary adenomas are tumors that occur in the pituitary gland, and account for about 10% of intracranial neoplasms. They often remain undiagnosed, and small pituitary tumors are found in 6 to 24 percent of adults at autopsy. ... 

absent pubic and axillary hair, delayed puberty, heart murmur, short stature

Turner syndrome encompasses several chromosomal abnormalities, of which monosomy X is the most common. It occurs in 1 out of every 2500 female births. Instead of the normal XX sex chromosomes for a female, only one X chromosome is present and fully functional. This is called 45,X or 45,X0, although other genetic variants occur. In Turner syndrome, female sexual characteristics are present but generally underdeveloped. ... 

blister(s) or bump(s) on back, cafe au lait spots, lump(s) in skin, pelvic pain

Neurofibromatosis type I (NF-1), also known as von Recklinghausen syndrome, comprises, along with neurofibromatosis type II (a.k.a. MISME syndrome), tuberous sclerosis, Sturge-Weber, and Von Hippel-Lindau disease, the phakomatoses or neurocutaneous syndromes, all of which have both neurologic and dermatologic lesions. This grouping is an artifact of an earlier time in medicine, before the distinct genetic basis of each of these disorders was understood. ... 

decreased eye movements, inability to judge depth, squint

Strabismus, commonly called lazy eye, is a condition in which the eyes are not properly aligned with each other. It typically involves a lack of coordination between the extraocular muscles that prevents bringing the gaze of each eye to the same point in space and preventing proper binocular vision, which may adversely affect depth perception. Strabismus can be either a disorder of the brain coordinating the eyes or a disorder of one or more muscles, as in any process that causes a dysfunction of the usual direction and power of the muscle or muscles. ... 

delayed development, face deformities, learning problems, short stature

Jacobsen Syndrome, also known as 11q deletion, is a rare congenital disorder resulting from deletion of a terminal region of chromosome 11 that includes band 11q24.1. It can cause mild mental retardation, a distinctive facial appearance, and a variety of physical problems including heart defects and a bleeding disorder. The syndrome was first identified by Danish physician Petra Jacobsen in 1973, and is believed to occur in approximately 1 out of every 100,000 births. ... 

face deformities, heart rate irregular, palpitations

Andersen-Tawil syndrome. also called Andersen syndrome and Long QT syndrome 7 is a form of long QT syndrome. It is a rare genetic disorder, and is inherited in an autosomal dominant pattern. ...